Rna interference in skin indications

ABSTRACT

The present invention relates to RNAi constructs with improved tissue and cellular uptake characteristics and methods of use of these compounds in dermal applications.

RELATED APPLICATIONS

This application claims the benefit under 35 U.S.C. § 119(e) of U.S. provisional application Ser. No. U.S. 61/192,954, entitled “Chemically Modified Polynucleotides and Methods of Using the Same,” filed on Sep. 22, 2008, U.S. 61/149,946, entitled “Minimum Length Triggers of RNA Interference,” filed on Feb. 4, 2009, and U.S. 61/224,031, entitled “Minimum Length Triggers of RNA Interference,” filed on Jul. 8, 2009, the disclosure of each of which is incorporated by reference herein in its entirety.

FIELD OF INVENTION

The invention pertains to the field of RNA interference (RNAi). The invention more specifically relates to nucleic acid molecules with improved in vivo delivery properties without the use of a delivering agent and their use in efficient gene silencing.

BACKGROUND OF INVENTION

Complementary oligonucleotide sequences are promising therapeutic agents and useful research tools in elucidating gene functions. However, prior art oligonucleotide molecules suffer from several problems that may impede their clinical development, and frequently make it difficult to achieve intended efficient inhibition of gene expression (including protein synthesis) using such compositions in vivo.

A major problem has been the delivery of these compounds to cells and tissues. Conventional double-stranded RNAi compounds, 19-29 bases long, form a highly negatively-charged rigid helix of approximately 1.5 by 10-15 nm in size. This rod type molecule cannot get through the cell-membrane and as a result has very limited efficacy both in vitro and in vivo. As a result, all conventional RNAi compounds require some kind of a delivery vehicle to promote their tissue distribution and cellular uptake. This is considered to be a major limitation of the RNAi technology.

There have been previous attempts to apply chemical modifications to oligonucleotides to improve their cellular uptake properties. One such modification was the attachment of a cholesterol molecule to the oligonucleotide. A first report on this approach was by Letsinger et al., in 1989. Subsequently, ISIS Pharmaceuticals, Inc. (Carlsbad, Calif.) reported on more advanced techniques in attaching the cholesterol molecule to the oilgonucleotide (Manoharan, 1992).

With the discovery of siRNAs in the late nineties, similar types of modifications were attempted on these molecules to enhance their delivery profiles. Cholesterol molecules conjugated to slightly modified (Soutschek, 2004) and heavily modified (Wolfrum, 2007) siRNAs appeared in the literature. Yamada et al., 2008 also reported on the use of advanced linker chemistries which further improved cholesterol mediated uptake of siRNAs. In spite of all this effort, the uptake of these types of compounds appears to be inhibited in the presence of biological fluids resulting in highly limited to efficacy in gene silencing in vivo, limiting the applicability of these compounds in a clinical setting.

Therefore, it would be of great benefit to improve upon the prior art oligonucleotides by designing oligonucleotides that have improved delivery properties in vivo and are clinically meaningful.

SUMMARY OF INVENTION

Described herein are asymmetric chemically modified nucleic acid molecules with minimal double stranded regions, and the use of such molecules in gene silencing. RNAi molecules associated with the invention contain single stranded regions and double stranded regions, and can contain a variety of chemical modifications within both the single stranded and double stranded regions of the molecule. Additionally, the RNAi molecules can be attached to a hydrophobic conjugate such as a conventional and advanced sterol-type molecule. This new class of RNAi molecules has superior efficacy both in vitro and in vivo than previously described RNAi molecules.

In some aspects the invention is a method involving administering a double stranded nucleic acid molecule selected from the nucleic acid molecules contained in Tables 1-3 such that an antisense and a sense strand make up the double stranded nucleic acid molecule, to a subject, wherein the nucleic acid molecule is administered on the skin of the subject.

In other aspects the invention is a method involving administering a double stranded nucleic acid molecule selected from the nucleic acid molecules contained in Tables 1-3 such that an antisense and a sense strand make up the double stranded nucleic acid molecule, to a subject, wherein the nucleic acid molecule is administered via intradermal injection.

A method for treating compromised skin is provided according to other aspects of the invention. The method involves administering to a subject a therapeutically effective amount for treating compromised skin of a double stranded nucleic acid molecule comprising a guide strand, with a minimal length of 16 nucleotides, and a passenger strand forming a double stranded nucleic acid, having a double stranded region and a single stranded region, the double stranded region having 8-15 nucleotides in length, the single stranded region having 4-12 nucleotides in length, wherein position 1 of the guide strand is 5′ phosphorylated or has a 2′ O-methyl modification, wherein the passenger strand is linked to a lipophilic group, wherein at least 40% of the nucleotides of the double stranded nucleic acid are modified, and wherein the double stranded nucleic acid molecule has one end that is blunt or includes a one nucleotide overhang.

In another aspect the invention is a method for delivering a nucleic acid to a subject by administering to a subject prior to or simultaneous with a medical procedure a therapeutically effective amount for treating compromised skin of a double stranded nucleic acid molecule comprising a guide strand, with a minimal length of 16 nucleotides, and a passenger strand forming a double stranded nucleic acid, having a double stranded region and a single stranded region, the double stranded region having 8-15 nucleotides in length, the single stranded region having 4-12 nucleotides in length, wherein position 1 of the guide strand is 5′ phosphorylated or has a 2′ O-methyl modification, wherein the passenger strand is linked to a lipophilic group, wherein at least 40% of the nucleotides of the double stranded nucleic acid are modified, and wherein the double stranded nucleic acid molecule has one end that is blunt or includes a one nucleotide overhang. In one embodiment the medical procedure is surgery. Optionally the surgery is elective.

A method for promoting wound healing is provided in another aspect. The method involves administering a therapeutically effective amount for promoting wound healing of a double stranded nucleic acid molecule comprising a guide strand, with a minimal length of 16 nucleotides, and a passenger strand forming a double stranded nucleic acid, having a double stranded region and a single stranded region, the double stranded region having 8-15 nucleotides in length, the single stranded region having 4-12 nucleotides in length, wherein position 1 of the guide strand is 5′ phosphorylated or has a 2′ O-methyl modification, wherein the passenger strand is linked to a lipophilic group, wherein at least 40% of the nucleotides of the double stranded nucleic acid are modified, and wherein the double stranded nucleic acid molecule has one end that is blunt or includes a one nucleotide overhang.

In some embodiments the subject has a wound, such as a chronic wound. The wound may be a result of elective surgery. In some embodiments the wound is external. In other embodiments the wound is internal.

The nucleic acid molecule may in some embodiments be administered before or after an injury. For example the nucleic acid molecule may be administered before or to after the injury via intradermal injection or locally to the skin.

In some embodiments the nucleic acid molecule is administered before a surgery. The surgery may be for instance epithelial grafting or skin grafting.

In some embodiments the nucleic acid molecule is administered to a graft donor site. In other embodiments the nucleic acid molecule is administered to a graft recipient site. In yet other embodiments the nucleic acid molecule is administered after burn injury.

Optionally the nucleic acid molecule may be administered prior to injury or surgery.

The double stranded nucleic acid molecule is directed against a gene encoding for a protein selected from the group consisting of: Transforming growth factor β (TGFβ1, TGFβ2), Osteopontin, Connective tissue growth factor (CTGF), Platelet-derived growth factor (PDGF), Hypoxia inducible factor-1α (HIF1α), Collagen I and/or III, Prolyl 4-hydroxylase (P4H), Procollagen C-protease (PCP), Matrix metalloproteinase 2, 9 (MMP2, 9), Integrins, Connexin, Histamine H1 receptor, Tissue transglutaminase, Mammalian target of rapamycin (mTOR), HoxB13, VEGF, IL-6, SMAD proteins, Ribosomal protein S6 kinases (RSP6) and Cyclooxygenase-2 (COX-2) in some embodiments.

In one embodiment the double stranded nucleic acid molecule is administered on the skin of the subject in need thereof. It may be in the form of a cream or ointment. In other embodiments the nucleic acid molecule is administered by local injection.

A composition of a double stranded nucleic acid molecule selected from the nucleic acid molecules contained in Tables 1-3 such that an antisense and a sense strand make up the double stranded nucleic acid molecule formulated for delivery to the skin is provided according to another aspect of the invention.

In another aspect the invention is a composition of a double stranded nucleic acid molecule comprising a guide strand, with a minimal length of 16 nucleotides, and a passenger strand forming a double stranded nucleic acid, having a double stranded region and a single stranded region, the double stranded region having 8-15 nucleotides in length, the single stranded region having 4-12 nucleotides in length, wherein position 1 of the guide strand is 5′ phosphorylated or has a 2′ O-methyl modification, wherein the passenger strand is linked to a lipophilic group, wherein at least 40% of the nucleotides of the double stranded nucleic acid are modified, and wherein the double stranded nucleic acid molecule has one end that is blunt or includes a one nucleotide overhang formulated for delivery to the skin. In one embodiment the nucleic acid molecule is in the form of a cream or ointment.

In some aspects the invention is methods for inhibiting scar tissue formation or for promoting epithelial regeneration. The methods involve administering a therapeutically effective amount for inhibiting scar tissue formation of a double stranded nucleic acid molecule selected from the nucleic acid molecules listed in Tables 1-3, to a subject in need thereof, to a subject in need thereof, to a subject in need thereof.

Alternatively the methods for inhibiting scar tissue formation or for promoting epithelial regeneration involve contacting epithelial cells with an effective amount for promoting epithelial regeneration of a double stranded nucleic acid molecule comprising a guide strand and a passenger strand, wherein the region of the molecule that is double stranded is from 8-14 nucleotides long, wherein the guide strand contains a single stranded region that is 4-12 nucleotides long, and wherein the single stranded region of the guide strand contains 2-12 phosphorothioate modifications, to a subject in need thereof.

Alternatively the methods for inhibiting scar tissue formation or for promoting epithelial regeneration involve administering to skin of a subject a therapeutically effective amount for inhibiting scar tissue formation or for promoting epithelial regeneration of a double stranded nucleic acid molecule comprising a guide strand, with a minimal length of 16 nucleotides, and a passenger strand forming a double stranded nucleic acid, having a double stranded region and a single stranded region, the double stranded region having 8-15 nucleotides in length, the single stranded region having 4-12 nucleotides in length, wherein position 1 of the guide strand is 5′ phosphorylated and/or has a 2′ O-methyl modification, wherein the passenger strand is linked to a lipophilic group, wherein at least 40% of the nucleotides of the double stranded nucleic acid are modified, and wherein the double stranded nucleic acid molecule has one end that is blunt or includes a one or two nucleotide overhang.

BRIEF DESCRIPTION OF DRAWINGS

The accompanying drawings are not intended to be drawn to scale. In the drawings, each identical or nearly identical component that is illustrated in various figures is represented by a like numeral. For purposes of clarity, not every component may be labeled in every drawing. In the drawings:

FIG. 1 is a schematic depicting proposed structures of asymmetric double stranded RNA molecules (adsRNA). Bold lines represent sequences carrying modification patterns compatible with RISC loading. Striped lines represent polynucleotides carrying modifications compatible with passenger strands. Plain lines represent a single stranded polynucleotide with modification patterns optimized for cell interaction and uptake. FIG. 1A depicts adsRNA with extended guide or passenger strands; FIG. 1B depicts adsRNA with length variations of a cell penetrating polynucleotide; FIG. 1C depicts adsRNA with 3′ and 5′ conjugates; FIG. 1D depicts adsRNAs with mismatches.

FIG. 2 is a schematic depicting asymmetric dsRNA molecules with different chemical modification patterns. Several examples of chemical modifications that might be used to increase hydrophobicity are shown including 4-pyridyl, 2-pyridyl, isobutyl and indolyl based position 5 uridine modifications.

FIG. 3 is a schematic depicting the use of dsRNA binding domains, protamine (or other Arg rich peptides), spermidine or similar chemical structures to block duplex charge to facilitate cellular entry.

FIG. 4 is a schematic depicting positively charged chemicals that might be used for polynucleotide charge blockage.

FIG. 5 is a schematic depicting examples of structural and chemical compositions of single stranded RISC entering polynucleotides. The combination of one or more modifications including 2′d, 2′Ome, 2′F, hydrophobic and phosphothioate modifications can be used to optimize single strand entry into the RISC.

FIG. 6 is a schematic depicting examples of structural and chemical composition of RISC substrate inhibitors. Combinations of one or more chemical modifications can be used to mediate efficient uptake and efficient binding to preloaded RISC complex.

FIG. 7 is a schematic depicting structures of polynucleotides with sterol type molecules attached, where R represent a polycarbonic tail of 9 carbons or longer. FIG. 7A depicts an adsRNA molecule; FIG. 7B depicts an siRNA molecule of approximately 17-30 bp long; FIG. 7C depicts a RISC entering strand; FIG. 7D depicts a substrate analog strand. Chemical modification patterns, as depicted in FIG. 7, can be optimized to promote desired function.

FIG. 8 is a schematic depicting examples of naturally occurring phytosterols with a polycarbon chain that is longer than 8, attached at position 17. More than 250 different types of phytosterols are known.

FIG. 9 is a schematic depicting examples of sterol-like structures, with variations in the size of the polycarbon chains attached at position 17.

FIG. 10 presents schematics and graphs demonstrating that the percentage of liver uptake and plasma clearance of lipid emulsions containing sterol type molecules is directly affected by the size of the polycarbon chain attached at position 17. This figure is adapted from Martins et al, Journal of Lipid Research (1998).

FIG. 11 is a schematic depicting micelle formation. FIG. 11A depicts a polynucleotide with a hydrophobic conjugate; FIG. 11B depicts linoleic acid; FIG. 11C depicts a micelle formed from a mixture of polynucleotides containing hydrophobic conjugates combined with fatty acids.

FIG. 12 is a schematic depicting how alteration in lipid composition can affect pharmacokinetic behavior and tissue distribution of hydrophobically modified and/or hydrophobically conjugated polynucleotides. In particular, use of lipid mixtures enriched in linoleic acid and cardiolipin results in preferential uptake by cardiomyocites.

FIG. 13 is a schematic showing examples of RNAi constructs and controls used to target MAP4K4 expression. RNAi construct 12083 corresponds to SEQ ID NOs:597 and 598. RNAi construct 12089 corresponds to SEQ ID NO:599.

FIG. 14 is a graph showing MAP4K4 expression following transfection with RNAi constructs associated with the invention. RNAi constructs tested were: 12083 (Nicked), 12085 (13nt Duplex), 12089 (No Stem Pairing) and 12134 (13nt miniRNA). Results of transfection were compared to an untransfected control sample. RNAi construct 12083 corresponds to SEQ ID NOs:597 and 598. RNAi construct 12085 corresponds to SEQ ID NOs:600 and 601. RNAi construct 12089 corresponds to SEQ ID NO:599. RNAi construct 12134 corresponds to SEQ ID NOs:602 and 603.

FIG. 15 is a graph showing expression of MAP4K4 24 hours post-transfection with RNAi constructs associated with the invention. RNAi constructs tested were: 11546 (MAP4K4 rxRNA), 12083 (MAP4K4 Nicked Construct), 12134 (12 bp soloRNA) and 12241 (14/3/14 soloRNA). Results of transfection were compared to a filler control sample. RNAi construct 11546 corresponds to SEQ ID NOs:604 and 605. RNAi construct 12083 corresponds to SEQ ID NOs:597 and 598. RNAi construct 12134 corresponds to SEQ ID NOs:602 and 603. RNAi construct 12241 corresponds to SEQ ID NOs:606 and 607.

FIG. 16 presents a graph and several tables comparing parameters associated with silencing of MAP4K4 expression following transfection with RNAi constructs associated with the invention. The rxRNA construct corresponds to SEQ ID NOs:604 and 605. The 14-3-14 soloRNA construct corresponds to SEQ ID NOs:606 and 607. The 13/19 duplex (nicked construct) corresponds to SEQ ID NOs:597 and 598. The 12-bp soloRNA construct corresponds to SEQ ID NOs:602 and 603.

FIG. 17 is a schematic showing examples of RNAi constructs and controls used to target SOD1 expression. The 12084 RNAi construct corresponds to SEQ ID NOs:612 and 613.

FIG. 18 is a graph showing SOD1 expression following transfection with RNAi constructs associated with the invention. RNAi constructs tested were: 12084 (Nicked), 12086 (13nt Duplex), 12090 (No Stem Pairing) and 12035 (13nt MiniRNA). Results of transfection were compared to an untransfected control sample. The 12084 RNAi construct corresponds to SEQ ID NOs:612 and 613. The 12086 RNAi construct corresponds to SEQ ID NOs:608 and 609. The 12035 RNAi construct corresponds to SEQ ID NOs:610 and 611.

FIG. 19 is a graph showing expression of SOD1 24 hours post-transfection with RNAi constructs associated with the invention. RNAi constructs tested were: 10015 (SOD1 rxRNA) and 12084 (SOD1 Nicked Construct). Results of transfection were compared to a filler control sample. The 10015 RNAi construct corresponds to SEQ ID NOs:614 and 615. The 12084 RNAi construct corresponds to SEQ ID NOs:612 and 613.

FIG. 20 is a schematic indicating that RNA molecules with double stranded regions that are less than 10 nucleotides are not cleaved by Dicer.

FIG. 21 is a schematic revealing a hypothetical RNAi model for RNA induced gene silencing.

FIG. 22 is a graph showing chemical optimization of asymmetric RNAi compounds. The presence of chemical modifications, in particular 2′F UC, phosphorothioate modifications on the guide strand, and complete CU 2′OMe modification of the passenger strands results in development of functional compounds. Silencing of MAP4K4 following lipid-mediated transfection is shown using RNAi molecules with specific modifications. RNAi molecules tested had sense strands that were 13 nucleotides long and contained the following modifications: unmodified; C and U 2′OMe; C and U 2′OMe and 3′ Chl; rxRNA 2′OMe pattern; or full 2′OMe, except base 1. Additionally, the guide (anti-sense) strands of the RNAi molecules tested contained the following modifications: unmodified; unmodified with 5′P; C and U 2′F; C and U 2′F with 8 PS 3′ end; and unmodified (17 nt length). Results for rxRNA 12/10 Duplex and negative controls are also shown.

FIG. 23 demonstrates that the chemical modifications described herein significantly increase in vitro efficacy in un-assisted delivery of RNAi molecules in HeLa cells. The structure and sequence of the compounds were not altered; only the chemical modification patterns of the molecules were modified. Compounds lacking 2′ F, 2′O-me, phosphorothioate modification, or cholesterol conjugates were completely inactive in passive uptake. A combination of all 4 of these types of modifications produced the highest levels of activity (compound 12386).

FIG. 24 is a graph showing MAP4K4 expression in Hela cells following passive uptake transfection of: NT Accell modified siRNA, MAP4K4 Accell siRNA, Non-Chl nanoRNA (12379) and sd-nanoRNA (12386).

FIG. 25 is a graph showing expression of MAP4K4 in HeLa cells following passive uptake transfection of various concentrations of RNA molecules containing the following parameters: Nano Lead with no 3′Chl; Nano Lead; Accell MAP4K4; 21mer GS with 8 PS tail; 21mer GS with 12 PS tail; and 25mer GS with 12 PS tail.

FIG. 26 is a graph demonstrating that reduction in oligonucleotide content increases the efficacy of unassisted uptake. Similar chemical modifications were applied to asymmetric compounds, traditional siRNA compounds and 25 mer RNAi compounds. The asymmetric small compounds demonstrated the most significant efficacy.

FIG. 27 is a graph demonstrating the importance of phosphorothioate content for un-assisted delivery. FIG. 27A demonstrates the results of a systematic screen that revealed that the presence of at least 2-12 phosphorothioates in the guide strand significantly improves uptake; in some embodiments, 4-8 phosphorothioate modifications were found to be preferred. FIG. 27B reveals that the presence or absence of phosphorothioate modifications in the sense strand did not alter efficacy.

FIG. 28 is a graph showing expression of MAP4K4 in primary mouse hepatocytes following passive uptake transfection of: Accell Media-Ctrl-UTC; MM APOB Alnylam; Active APOB Alnylam; nanoRNA without chl; nanoRNA MAP4K4; Mouse MAP4K4 Accell Smartpool; DY547 Accell Control; Luc Ctrl rxRNA with Dy547; MAP4K4 rxRNA with DY547; and AS Strand Alone (nano).

FIG. 29 is a graph showing expression of ApoB in mouse primary hepatocytes following passive uptake transfection of: Accell Media-Ctrl-UTC; MM APOB Alnylam; Active APOB Alnylam; nanoRNA without chl; nanoRNA MAP4K4; Mouse MAP4K4 Accell Smartpool; DY547 Accell Control; Luc Ctrl rxRNA with Dy547; MAP4K4 rxRNA with DY547; and AS Strand Alone (nano).

FIG. 30 is a graph showing expression of MAP4K4 in primary human hepatocytes following passive uptake transfection of: 11550 MAP4K4 rxRNA; 12544 MM MAP4K4 nanoRNA; 12539 Active MAP4K4 nanoRNA; Accell Media; and UTC.

FIG. 31 is a graph showing ApoB expression in primary human hepatoctyes following passive uptake transfection of: 12505 Active ApoB chol-siRNA; 12506 MM ApoB chol-siRNA; Accell Media; and UTC.

FIG. 32 is an image depicting localization of sd-rxRNA^(nano) localization.

FIG. 33 is an image depicting localization of Chol-siRNA (Alnylam).

FIG. 34 is a schematic of 1^(st) generation (G1) sd-rxRNA^(nano) molecules associated with the invention indicating regions that are targeted for modification, and functions associated with different regions of the molecules.

FIG. 35 depicts modification patterns that were screened for optimization of sd-rxRNA^(nano) (G1). The modifications that were screened included, on the guide strand, lengths of 19, 21 and 25 nucleotides, phosphorothioate modifications of 0-18 nucleotides, and replacement of 2′F modifications with 2′OMe, 5 Methyl C and/or ribo Thymidine modifications. Modifications on the sense strand that were screened included nucleotide lengths of 11, 13 and 19 nucleotides, phosphorothiote modifications of 0-4 nucleotides and 2′OMe modifications.

FIG. 36 is a schematic depicting modifications of sd-rxRNAN^(nano) that were screened for optimization.

FIG. 37 is a graph showing percent MAP4K4 expression in Hek293 cells following transfection of: Risc Free siRNA; rxRNA; Nano (unmodified); GS alone; Nano Lead (no Chl); Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 8 PS, 19 nt); Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 8 PS, 21 nt); Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 12 PS, 21 nt); and Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 12 PS, 25 nt);

FIG. 38 is a graph showing percent MAP4K4 expression in HeLa cells following passive uptake transfection of: GS alone; Nano Lead; Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 8 PS, 19 nt); Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 8 PS, 21 nt); Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 12 PS, 21 nt); Nano (GS: (3) 2′OMe at positions 1, 18, and 19, 12 PS, 25 nt).

FIG. 39 is a graph showing percent MAP4K4 expression in Hek293 cells following lipid mediated transfection of: Guide Strand alone (GS: 8PS, 19 nt); Guide Strand alone (GS: 18PS, 19 nt); Nano (GS: no PS, 19 nt); Nano (GS: 2 PS, 19 nt); Nano (GS: 4 PS, 19 nt); Nano (GS: 6 PS, 19 nt); Nano Lead (GS: 8 PS, 19 nt); Nano (GS: 10 PS, 19 nt); Nano (GS: 12 PS, 19 nt); and Nano (GS: 18 PS, 19 nt).

FIG. 40 is a graph showing percent MAP4K4 expression in Hek293 cells following lipid mediated transfection of: Guide Strand alone (GS: 8PS, 19 nt); Guide Strand alone (GS: 18PS, 19 nt); Nano (GS: no PS, 19 nt); Nano (GS: 2 PS, 19 nt); Nano (GS: 4 PS, 19 nt); Nano (GS: 6 PS, 19 nt); Nano Lead (GS: 8 PS, 19 nt); Nano (GS: 10 PS, 19 nt); Nano (GS: 12 PS, 19 nt); and Nano (GS: 18 PS, 19 nt).

FIG. 41 is a graph showing percent MAP4K4 expression in HeLa cells following passive uptake transfection of: Nano Lead (no Chl); Guide Strand alone (18 PS); Nano (GS: 0 PS, 19 nt); Nano (GS: 2 PS, 19 nt); Nano (GS: 4 PS, 19 nt); Nano (GS: 6 PS, 19 nt); Nano Lead (GS: 8 PS, 19 nt); Nano (GS: 10 PS, 19 nt); Nano (GS: 12 PS, 19 nt); and Nano (GS: 18 PS, 19 nt).

FIG. 42 is a graph showing percent MAP4K4 expression in HeLa cells following passive uptake transfection of: Nano Lead (no Chl); Guide Strand alone (18 PS); Nano (GS: 0 PS, 19 nt); Nano (GS: 2 PS, 19 nt); Nano (GS: 4 PS, 19 nt); Nano (GS: 6 PS, 19 nt); Nano Lead (GS: 8 PS, 19 nt); Nano (GS: 10 PS, 19 nt); Nano (GS: 12 PS, 19 nt); and Nano (GS: 18 PS, 19 nt).

FIG. 43 is a schematic depicting guide strand chemical modifications that were screened for optimization.

FIG. 44 is a graph showing percent MAP4K4 expression in Hek293 cells following reverse transfection of: RISC free siRNA; GS only (2′F C and Us); GS only (2′OMe C and Us); Nano Lead (2′F C and Us); nano (GS: (3) 2′OMe, positions 16-18); nano (GS: (3) 2′OMe, positions 16, 17 and 19); nano (GS: (4) 2′OMe, positions 11, 16-18); nano (GS: (10) 2′OMe,C and Us); nano (GS: (6) 2′OMe, positions 1 and 5-9); nano (GS: (3) 2′OMe, positions 1, 18 and 19); and nano (GS: (5) 2′OMe Cs).

FIG. 45 is a graph demonstrating efficacy of various chemical modification patterns. In particular, 2-OMe modification in positions 1 and 11-18 was well tolerated. 2′OMe modifications in the seed area resulted in a slight reduction of efficacy (but were still highly efficient). Ribo-modifications in the seed were well tolerated. This data enabled the generation of self delivering compounds with reduced or no 2′F modifications. This is significant because 2′F modifications may be associated with toxicity in vivo.

FIG. 46 is a schematic depicting sense strand modifications.

FIG. 47 is a graph demonstrating sense strand length optimization. A sense strand length between 10-15 bases was found to be optimal in this assay. Increasing sense strand length resulted in a reduction of passive uptake of these compounds but may be tolerated for other compounds. Sense strands containing LNA modification demonstrated similar efficacy to non-LNA containing compounds. In some embodiments, the addition of LNA or other thermodynamically stabilizing compounds can be beneficial, resulting in converting non-functional sequences into functional sequences.

FIG. 48 is a graph showing percent MAP4K4 expression in HeLa cells following passive uptake transfection of: Guide Strand Alone (2′F C and U); Nano Lead; Nano Lead (No Chl); Nano (SS: 11 nt 2′OMe C and Us, Chl); Nano (SS: 11nt, complete 2′OMe, Chl); Nano (SS: 19 nt, 2′OMe C and Us, Chl); Nano (SS: 19 nt, 2′OMe C and Us, no Chl).

FIG. 49 is a graph showing percent MAP4K4 expression in HeLa cells following passive uptake transfection of: Nano Lead (No Chl); Nano (SS no PS); Nano Lead (SS:2 PS); Nano (SS:4 PS).

FIG. 50 is a schematic depicting a sd-rxRNA^(nano) second generation (GII) lead molecule.

FIG. 51 presents a graph indicating EC50 values for MAP4K4 silencing in the presence of sd-rxRNA, and images depicting localization of DY547-labeled rxRNA^(ori) and DY547-labeled sd-rxRNA.

FIG. 52 is a graph showing percent MAP4K4 expression in HeLa cells in the presence of optimized sd-rxRNA molecules.

FIG. 53 is a graph depicting the relevance of chemistry content in optimization of sd-rxRNA efficacy.

FIG. 54 presents schematics of sterol-type molecules and a graph revealing that sd-rxRNA compounds are fully functional with a variety of linker chemistries. GII asymmetric compounds were synthesized with sterol type molecules attached through TEG and amino caproic acid linkers. Both linkers showed identical potency. This functionality independent of linker chemistry indicates a significant difference between the molecules described herein and previously described molecules, and offers significant advantages for the molecules described herein in terms of scale up and synthesis.

FIG. 55 demonstrates the stability of chemically modified sd-rxRNA compounds in human serum in comparison to non modified RNA. The oligonucleotides were incubated in 75% serum at 37° C. for the number of hours indicated. The level of degradation was determined by running the samples on non-denaturing gels and staining with SYBGR.

FIG. 56 is a graph depicting optimization of cellular uptake of sd-rxRNA through minimizing oligonucleotide content.

FIG. 57 is a graph showing percent MAP4K4 expression after spontaneous cellular uptake of sd-rxRNA in mouse PEC-derived macrophages, and phase and fluorescent images showing localization of sd-rxRNA.

FIG. 58 is a graph showing percent MAP4K4 expression after spontaneous cellular uptake of sd-rxRNA (targeting) and sd-rxRNA (mismatch) in mouse primary hepatocytes, and phase and fluorescent images showing localization of sd-rxRNA.

FIG. 59 presents images depicting localization of DY547-labeled sd-rxRNA delivered to RPE cells with no formulation.

FIG. 60 is a graph showing silencing of MAP4K4 expression in RPE cells treated with sd-rxRNA^(nano) without formulation.

FIG. 61 presents a graph and schematics of RNAi compounds showing the chemical/structural composition of highly effective sd-rxRNA compounds. Highly effective compounds were found to have the following characteristics: antisense strands of 17-21 nucleotides, sense strands of 10-15 nucleotides, single-stranded regions that contained 2-12 phosphorothioate modifications, preferentially 6-8 phosphorothioate modifications, and sense strands in which the majority of nucleotides were 2′OMe modified, with or without phosphorothioate modification. Any linker chemistry can be used to attach these molecules to hydrophobic moieties such as cholesterol at the 3′ end of the sense strand. Version GIIa-b of these RNA compounds demonstrate that elimination of 2′F content has no impact on efficacy.

FIG. 62 presents a graph and schematics of RNAi compounds demonstrating the superior performance of sd-rxRNA compounds compared to compounds published by Wolfrum et. al. Nature Biotech, 2007. Both generation I and II compounds (GI and GIIa) developed herein show great efficacy. By contrast, when the chemistry described in Wolfrum et al. (all oligos contain cholesterol conjugated to the 3′ end of the sense strand) was applied to the same sequence in a context of conventional siRNA (19 bp duplex with two overhang) the compound was practically inactive. These data emphasize the significance of the combination of chemical modifications and assymetrical molecules described herein, producing highly effective RNA compounds.

FIG. 63 presents images showing that sd-rxRNA accumulates inside cells while other less effective conjugate RNAs accumulate on the surface of cells.

FIG. 64 presents images showing that sd-rxRNA molecules, but not other molecules, are internalized into cells within minutes.

FIG. 65 presents images demonstrating that sd-rxRNA compounds have drastically better cellular and tissue uptake characteristics when compared to conventional cholesterol conjugated siRNAs (such as those published by Soucheck et al). FIG. 65A,B compare uptake in RPE cells, FIG. 65C,D compare uptake upon local administration to skin and FIG. 65E,F compare uptake by the liver upon systemic administration. The level of uptake is at least an order of magnitude higher for the sd-rxRNA compounds relative to the regular siRNA-cholesterol compounds.

FIG. 66 presents images depicting localization of rxRNA^(ori) and sd-rxRNA following local delivery.

FIG. 67 presents images depicting localization of sd-rxRNA and other conjugate RNAs following local delivery.

FIG. 68 presents a graph revealing the results of a screen performed with sd-rxRNAGII chemistry to identify functional compounds targeting the SPP1 gene. Multiple effective compounds were identified, with 14131 being the most effective. The compounds were added to A-549 cells and the level of the ratio of SPP1/PPIB was determined by B-DNA after 48 hours.

FIG. 69 presents a graph and several images demonstrating efficient cellular uptake of sd-rxRNA within minutes of exposure. This is a unique characteristics of the sd-rxRNA compounds described herein, not observed with any other RNAi compounds. The Soutschek et al. compound was used as a negative control.

FIG. 70 presents a graph and several images demonstrating efficient uptake and silencing of sd-rxRNA compounds in multiple cell types with multiple sequences. In each case silencing was confirmed by looking at target gene expression using a Branched DNA assay.

FIG. 71 presents a graph revealing that sd-rxRNA is active in the presence and absence of serum. A slight reduction in efficacy (2-5 fold) was observed in the presence of serum. This minimal reduction in efficacy in the presence of serum differentiates the sd-rxRNA compounds described herein from previously described RNAi compounds, which had a greater reduction in efficacy, and thus creates a foundation for in vivo efficacy of the sd-rxRNA molecules described herein.

FIG. 72 presents images demonstrating efficient tissue penetration and cellular uptake upon single intradermal injection of sd-rxRNA compounds described herein. This represents a model for local delivery of sd-rxRNA compounds as well as an effective demonstration of delivery of sd-rxRNA compounds and silencing of genes in dermatological applications.

FIG. 73 presents images and a graph demonstrating efficient cellular uptake and in vivo silencing with sd-rxRNA following intradermal injection.

FIG. 74 presents graphs demonstrating that sd-rxRNA compounds have improved blood clearance and induce effective gene silencing in vivo in the liver upon systemic administration.

FIG. 75 presents a graph demonstrating that the presence of 5-Methyl C in an RNAi compound resulted in an increase in potency of lipid mediated transfection, demonstrating that hydrophobic modification of Cs and Us in the content of RNAi compounds can be beneficial. In some embodiments, these types of modifications can be used in the context of 2′ ribose modified bases to insure optimal stability and efficacy.

FIG. 76 presents a graph showing percent MAP4K4 expression in HeLa cells following passive uptake transfection of: Guide strand alone; Nano Lead; Nano Lead (No cholesterol); Guide Strand w/5MeC and 2′F Us Alone; Nano Lead w/GS SMeC and 2′F Us; Nano Lead w/GS riboT and 5 Methyl Cs; and Nano Lead w/Guide dT and 5 Methyl Cs.

FIG. 77 presents images comparing localization of sd-rxRNA and other RNA conjugates following systemic delivery to the liver.

FIG. 78 presents schematics demonstrating 5-uridyl modifications with improved hydrophobicity characteristics. Incorporation of such modifications into sd-rxRNA compounds can increase cellular and tissue uptake properties. FIG. 78B presents a new type of RNAi compound modification which can be applied to compounds to improve cellular uptake and pharmacokinetic behavior. This type of modification, when applied to sd-rxRNA compounds, may contribute to making such compounds orally available.

FIG. 79 presents schematics revealing the structures of synthesized modified sterol type molecules, where the length and structure of the C17 attached tail is modified. Without wishing to be bound by any theory, the length of the C17 attached tail may contribute to improving in vitro and in vivo efficacy of sd-rxRNA compounds.

FIG. 80 presents a schematic demonstrating the lithocholic acid route to long side chain cholesterols.

FIG. 81 presents a schematic demonstrating a route to 5-uridyl phosphoramidite synthesis.

FIG. 82 presents a schematic demonstrating synthesis of tri-functional hydroxyprolinol linker for 3′-cholesterol attachment.

FIG. 83 presents a schematic demonstrating synthesis of solid support for the manufacture of a shorter asymmetric RNAi compound strand.

FIG. 84 demonstrates SPPI sd-rxRNA compound selection. Sd-rxRNA compounds targeting SPP1 were added to A549 cells (using passive transfection) and the level of SPP1 expression was evaluated after 48 hours. Several novel compounds effective in SPP1 silencing were identified, the most potent of which was compound 14131.

FIG. 85 demonstrates independent validation of sd-rxRNA compounds 14116, 14121, 14131, 14134, 14139, 14149, and 14152 efficacy in SPP1 silencing.

FIG. 86 demonstrates results of sd-rxRNA compound screens to identify sd-rxRNA compounds functional in CTGF knockdown.

FIG. 87 demonstrates results of sd-rxRNA compound screens to identify sd-rxRNA functional in CTGF knockdown.

FIG. 88 demonstrates a systematic screen identifying the minimal length of the asymmetric compounds. The passenger strand of 10-19 bases was hybridized to a guide strand of 17-25 bases. In this assay, compounds with duplex regions as short as 10 bases were found to be effective in inducing.

FIG. 89 demonstrates that positioning of the sense strand relative to the guide strand is critical for RNAi Activity. In this assay, a blunt end was found to be optimal, a 3′ overhang was tolerated, and a 5′ overhang resulted in complete loss of functionality.

FIG. 90 demonstrates that the guide strand, which has homology to the target only at nucleotides 2-17, resulted in effective RNAi when hybridized with sense strands of different lengths. The compounds were introduced into HeLa cells via lipid mediated transfection.

FIG. 91 is a schematic depicting a panel of sterol-type molecules which can be used as a hydrophobic entity in place of cholesterol. In some instances, the use of sterol-type molecules comprising longer chains results in generation of sd-rxRNA compounds with significantly better cellular uptake and tissue distribution properties.

FIG. 92 presents schematics depicting a panel of hydrophobic molecules which might be used as a hydrophobic entity in place of cholesterol. These list just provides representative examples; any small molecule with substantial hydrophobicity can be used.

DETAILED DESCRIPTION

Aspects of the invention relate to methods and compositions involved in gene silencing. The invention is based at least in part on the surprising discovery that asymmetric nucleic acid molecules with a double stranded region of a minimal length such as 8-14 nucleotides, are effective in silencing gene expression. Molecules with such a short double stranded region have not previously been demonstrated to be effective in mediating RNA interference. It had previously been assumed that that there must be a double stranded region of 19 nucleotides or greater. The molecules described herein are optimized through chemical modification, and in some instances through attachment of hydrophobic conjugates.

The invention is based at least in part on another surprising discovery that asymmetric nucleic acid molecules with reduced double stranded regions are much more effectively taken up by cells compared to conventional siRNAs. These molecules are highly efficient in silencing of target gene expression and offer significant advantages over previously described RNAi molecules including high activity in the presence of serum, efficient self delivery, compatibility with a wide variety of linkers, and reduced presence or complete absence of chemical modifications that are associated with toxicity.

In contrast to single-stranded polynucleotides, duplex polynucleotides have been difficult to deliver to a cell as they have rigid structures and a large number of negative charges which makes membrane transfer difficult. Unexpectedly, it was found that the polynucleotides of the present invention, although partially double-stranded, are recognized in vivo as single-stranded and, as such, are capable of efficiently being delivered across cell membranes. As a result the polynucleotides of the invention are capable in many instances of self delivery. Thus, the polynucleotides of the invention may be formulated in a manner similar to conventional RNAi agents or they may be delivered to the cell or subject alone (or with non-delivery type carriers) and allowed to self deliver. In one embodiment of the present invention, self delivering asymmetric double-stranded RNA molecules are provided in which one portion of the molecule resembles a conventional RNA duplex and a second portion of the molecule is single stranded.

The polynucleotides of the invention are referred to herein as isolated double stranded or duplex nucleic acids, oligonucleotides or polynucleotides, nano molecules, nano RNA, sd-rxRNA^(nano), sd-rxRNA or RNA molecules of the invention.

The oligonucleotides of the invention in some aspects have a combination of asymmetric structures including a double stranded region and a single stranded region of 5 nucleotides or longer, specific chemical modification patterns and are conjugated to lipophilic or hydrophobic molecules. This new class of RNAi like compounds have superior efficacy in vitro and in vivo. Based on the data described herein it is believed that the reduction in the size of the rigid duplex region in combination with phosphorothioate modifications applied to a single stranded region are new and important for achieving the observed superior efficacy. Thus, the RNA molecules described herein are different in both structure and composition as well as in vitro and in vivo activity.

In a preferred embodiment the RNAi compounds of the invention comprise an asymmetric compound comprising a duplex region (required for efficient RISC entry of 10-15 bases long) and single stranded region of 4-12 nucleotides long; with a 13 nucleotide duplex. A 6 nucleotide single stranded region is preferred in some embodiments. The single stranded region of the new RNAi compounds also comprises 2-12 phosphorothioate internucleotide linkages (referred to as phosphorothioate modifications). 6-8 phosphorothioate internucleotide linkages are preferred in some embodiments. Additionally, the RNAi compounds of the invention also include a unique chemical modification pattern, which provides stability and is compatible with RISC entry. The combination of these elements has resulted in unexpected properties which are highly useful for delivery of RNAi reagents in vitro and in vivo.

The chemically modification pattern, which provides stability and is compatible with RISC entry includes modifications to the sense, or passenger, strand as well as the antisense, or guide, strand. For instance the passenger strand can be modified with any chemical entities which confirm stability and do not interfere with activity. Such modifications include 2′ ribo modifications (O-methyl, 2′ F, 2 deoxy and others) and backbone modification like phosphorothioate modifications. A preferred chemical modification pattern in the passenger strand includes Omethyl modification of C and U nucleotides within the passenger strand or alternatively the passenger strand may be completely Omethyl modified.

The guide strand, for example, may also be modified by any chemical modification which confirms stability without interfering with RISC entry. A preferred chemical modification pattern in the guide strand includes the majority of C and U nucleotides being 2′ F modified and the 5′ end being phosphorylated. Another preferred chemical modification pattern in the guide strand includes 2′Omethyl modification of position 1 and C/U in positions 11-18 and 5′ end chemical phosphorylation. Yet another preferred chemical modification pattern in the guide strand includes 2′Omethyl modification of position 1 and C/U in positions 11-18 and 5′ end chemical phosphorylation and 2′F modification of C/U in positions 2-10.

It was surprisingly discovered according to the invention that the above-described chemical modification patterns of the oligonucleotides of the invention are well tolerated and actually improved efficacy of asymmetric RNAi compounds. See, for instance, FIG. 22.

It was also demonstrated experimentally herein that the combination of modifications to RNAi when used together in a polynucleotide results in the achievement of optimal efficacy in passive uptake of the RNAi. Elimination of any of the described components (Guide strand stabilization, phosphorothioate stretch, sense strand stabilization and hydrophobic conjugate) or increase in size results in sub-optimal efficacy and in some instances complete lost of efficacy. The combination of elements results in development of compound, which is fully active following passive delivery to cells such as HeLa cells. (FIG. 23). The degree to which the combination of elements results in efficient self delivery of RNAi molecules was completely unexpected.

The data shown in FIGS. 26, 27 and 43 demonstrated the importance of the various modifications to the RNAi in achieving stabilization and activity. For instance, FIG. 26 demonstrates that use off asymmetric configuration is important in getting efficacy in passive uptake. When the same chemical composition is applied to compounds of traditional configurations (19-21 bases duplex and 25 mer duplex) the efficacy was drastically decreased in a length dependent manner. FIG. 27 demonstrated a systematic screen of the impact of phosphorothioate chemical modifications on activity. The sequence, structure, stabilization chemical modifications, hydrophobic conjugate were kept constant and compound phosphorothioate content was varied (from 0 to 18 PS bond). Both compounds having no phosphorothioate linkages and having 18 phosphorothioate linkages were completely inactive in passive uptake. Compounds having 2-16 phosphorothioate linkages were active, with compounds having 4-10 phosphorothioate being the most active compounds.

The data in the Examples presented below demonstrates high efficacy of the oligonucleotides of the invention both in vitro in variety of cell types (supporting data) and in vivo upon local and systemic administration. For instance, the data compares the ability of several competitive RNAi molecules having different chemistries to silence a gene. Comparison of sd-rxRNA (oligonucleotides of the invention) with RNAs described in Soucheck et al. and Wolfrum at al., as applied to the same targeting region, demonstrated that only sd-rxRNA chemistry showed a significant functionality in passive uptake. The composition of the invention achieved EC50 values of 10-50 pM. This level of efficacy is un-attainable with conventional chemistries like those described in Sauthceck at al and Accell. Similar comparisons were made in other systems, such as in vitro (RPE cell line), in vivo upon local administration (wounded skin) and systemic (50 mg/kg) as well as other genes (FIGS. 65 and 68). In each case the oligonucleotides of the invention achieved better results. FIG. 64 includes data demonstrating efficient cellular uptake and resulting silencing by sd-rxRNA compounds only after 1 minute of exposure. Such an efficacy is unique to this composition and have not been seen with other types of molecules in this class. FIG. 70 demonstrates efficient uptake and silencing of sd-rxRNA compounds in multiple cell types with multiple sequences. The sd-rxRNA compounds are also active in cells in presence and absence of serum and other biological liquids. FIG. 71 demonstrates only a slight reduction in activity in the presence of serum. This ability to function in biologically aggressive environment effectively further differentiates sd-rxRNA compounds from other compounds described previously in this group, like Accell and Soucheck et al, in which uptake is drastically inhibited in a presence of serum.

Significant amounts of data also demonstrate the in vivo efficacy of the compounds of the invention. For instance FIGS. 72-74 involve multiple routes of in vivo delivery of the compounds of the invention resulting in significant activity. FIG. 72, for example, demonstrates efficient tissue penetration and cellular uptake upon single intradermal injection. This is a model for local delivery of sd-rxRNA compounds as well as an effective delivery mode for sd-rxRNA compounds and silencing genes in any dermatology applications. FIG. 73 demonstrated efficient tissue penetration, cellular uptake and silencing upon local in vivo intradermal injection of sd-rxRNA compounds. The data of FIG. 74 demonstrate that sd-rxRNA compounds result in highly effective liver uptake upon IV administration. Comparison to Souicheck at al molecule showed that the level of liver uptake at identical dose level was quite surprisingly, at least 50 fold higher with the sd-rxRNA compound than the Souicheck at al molecule.

The sd-rxRNA can be further improved in some instances by improving the hydrophobicity of compounds using of novel types of chemistries. For example one chemistry is related to use of hydrophobic base modifications. Any base in any position might be modified, as long as modification results in an increase of the partition coefficient of the base. The preferred locations for modification chemistries are positions 4 and 5 of the pyrimidines. The major advantage of these positions is (a) ease of synthesis and (b) lack of interference with base-pairing and A form helix formation, which are essential for RISC complex loading and target recognition. Examples of these chemistries is shown in FIGS. 75-83. A version of sd-rxRNA compounds where multiple deoxy Uridines are present without interfering with overall compound efficacy was used. In addition major improvement in tissue distribution and cellular uptake might be obtained by optimizing the structure of the hydrophobic conjugate. In some of the preferred embodiment the structure of sterol is modified to alter (increase/decrease) C17 attached chain. This type of modification results in significant increase in cellular uptake and improvement of tissue uptake prosperities in vivo.

This invention is not limited in its application to the details of construction and the arrangement of components set forth in the following description or illustrated in the drawings. The invention is capable of other embodiments and of being practiced or of being carried out in various ways. Also, the phraseology and terminology used herein is for the purpose of description and should not be regarded as limiting. The use of “including,” “comprising,” or “having,” “containing,” “involving,” and variations thereof herein, is meant to encompass the items listed thereafter and equivalents thereof as well as additional items.

Thus, aspects of the invention relate to isolated double stranded nucleic acid molecules comprising a guide (antisense) strand and a passenger (sense) strand. As used herein, the term “double-stranded” refers to one or more nucleic acid molecules in which at least a portion of the nucleomonomers are complementary and hydrogen bond to form a double-stranded region. In some embodiments, the length of the guide strand ranges from 16-29 nucleotides long. In certain embodiments, the guide strand is 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, or 29 nucleotides long. The guide strand has complementarity to a target gene. Complementarity between the guide strand and the target gene may exist over any portion of the guide strand. Complementarity as used herein may be perfect complementarity or less than perfect complementarity as long as the guide strand is sufficiently complementary to the target that it mediates RNAi. In some embodiments complementarity refers to less than 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2%, or 1% mismatch between the guide strand and the target. Perfect complementarity refers to 100% complementarity. Thus the invention has the advantage of being able to tolerate sequence variations that might be expected due to genetic mutation, strain polymorphism, or evolutionary divergence. For example, siRNA sequences with insertions, deletions, and single point mutations relative to the target sequence have also been found to be effective for inhibition. Moreover, not all positions of a siRNA contribute equally to target recognition. Mismatches in the center of the siRNA are most critical and essentially abolish target RNA cleavage. Mismatches upstream of the center or upstream of the cleavage site referencing the antisense strand are tolerated but significantly reduce target RNA cleavage. Mismatches downstream of the center or cleavage site referencing the antisense strand, preferably located near the 3′ end of the antisense strand, e.g. 1, 2, 3, 4, 5 or 6 nucleotides from the 3′ end of the antisense strand, are tolerated and reduce target RNA cleavage only slightly.

While not wishing to be bound by any particular theory, in some embodiments, the guide strand is at least 16 nucleotides in length and anchors the Argonaute protein in RISC. In some embodiments, when the guide strand loads into RISC it has a defined seed region and target mRNA cleavage takes place across from position 10-11 of the guide strand. In some embodiments, the 5′ end of the guide strand is or is able to be phosphorylated. The nucleic acid molecules described herein may be referred to as minimum trigger RNA.

In some embodiments, the length of the passenger strand ranges from 8-14 nucleotides long. In certain embodiments, the passenger strand is 8, 9, 10, 11, 12, 13 or 14 nucleotides long. The passenger strand has complementarity to the guide strand. Complementarity between the passenger strand and the guide strand can exist over any portion of the passenger or guide strand. In some embodiments, there is 100% complementarity between the guide and passenger strands within the double stranded region of the molecule.

Aspects of the invention relate to double stranded nucleic acid molecules with minimal double stranded regions. In some embodiments the region of the molecule that is double stranded ranges from 8-14 nucleotides long. In certain embodiments, the region of the molecule that is double stranded is 8, 9, 10, 11, 12, 13 or 14 nucleotides long. In certain embodiments the double stranded region is 13 nucleotides long. There can be 100% complementarity between the guide and passenger strands, or there may be one or more mismatches between the guide and passenger strands. In some embodiments, on one end of the double stranded molecule, the molecule is either blunt-ended or has a one-nucleotide overhang. The single stranded region of the molecule is in some embodiments between 4-12 nucleotides long. For example the single stranded region can be 4, 5, 6, 7, 8, 9, 10, 11 or 12 nucleotides long. However, in certain embodiments, the single stranded region can also be less than 4 or greater than 12 nucleotides long. In certain embodiments, the single stranded region is 6 nucleotides long.

RNAi constructs associated with the invention can have a thermodynamic stability (ΔG) of less than −13 kkal/mol. In some embodiments, the thermodynamic stability (ΔG) is less than −20 kkal/mol. In some embodiments there is a loss of efficacy when (ΔG) goes below −21 kkal/mol. In some embodiments a (ΔG) value higher than −13 kkal/mol is compatible with aspects of the invention. Without wishing to be bound by any theory, in some embodiments a molecule with a relatively higher (ΔG) value may become active at a relatively higher concentration, while a molecule with a relatively lower (ΔG) value may become active at a relatively lower concentration. In some embodiments, the (ΔG) value may be higher than −9 kkcal/mol. The gene silencing effects mediated by the RNAi constructs associated with the invention, containing minimal double stranded regions, are unexpected because molecules of almost identical design but lower thermodynamic stability have been demonstrated to be inactive (Rana et al. 2004).

Without wishing to be bound by any theory, results described herein suggest that a stretch of 8-10 bp of dsRNA or dsDNA will be structurally recognized by protein components of RISC or co-factors of RISC. Additionally, there is a free energy requirement for the triggering compound that it may be either sensed by the protein components and/or stable enough to interact with such components so that it may be loaded into the Argonaute protein. If optimal thermodynamics are present and there is a double stranded portion that is preferably at least 8 nucleotides then the duplex will be recognized and loaded into the RNAi machinery.

In some embodiments, thermodynamic stability is increased through the use of LNA bases. In some embodiments, additional chemical modifications are introduced. Several non-limiting examples of chemical modifications include: 5′ Phosphate, 2′-O-methyl, 2′-O-ethyl, 2′-fluoro, ribothymidine, C-5 propynyl-dC (pdC) and C-5 propynyl-dU (pdU); C-5 propynyl-C (pC) and C-5 propynyl-U (pU); 5-methyl C, 5-methyl U, 5-methyl dC, 5-methyl dU methoxy, (2,6-diaminopurine), 5′-Dimethoxytrityl-N4-ethyl-2′-deoxyCytidine and MGB (minor groove binder). It should be appreciated that more than one chemical modification can be combined within the same molecule.

Molecules associated with the invention are optimized for increased potency and/or reduced toxicity. For example, nucleotide length of the guide and/or passenger strand, and/or the number of phosphorothioate modifications in the guide and/or passenger strand, can in some aspects influence potency of the RNA molecule, while replacing 2′-fluoro (2′F) modifications with 2′-O-methyl (2′OMe) modifications can in some aspects influence toxicity of the molecule. Specifically, reduction in 2′F content of a molecule is predicted to reduce toxicity of the molecule. The Examples section presents molecules in which 2′F modifications have been eliminated, offering an advantage over previously described RNAi compounds due to a predicted reduction in toxicity. Furthermore, the number of phosphorothioate modifications in an RNA molecule can influence the uptake of the molecule into a cell, for example the efficiency of passive uptake of the molecule into a cell. Preferred embodiments of molecules described herein have no 2′F modification and yet are characterized by equal efficacy in cellular uptake and tissue penetration. Such molecules represent a significant improvement over prior art, such as molecules described by Accell and Wolfrum, which are heavily modified with extensive use of 2′F.

In some embodiments, a guide strand is approximately 18-19 nucleotides in length and has approximately 2-14 phosphate modifications. For example, a guide strand can contain 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or more than 14 nucleotides that are phosphate-modified. The guide strand may contain one or more modifications that confer increased stability without interfering with RISC entry. The phosphate modified nucleotides, such as phosphorothioate modified nucleotides, can be at the 3′ end, 5′ end or spread throughout the guide strand. In some embodiments, the 3′ terminal 10 nucleotides of the guide strand contains 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 phosphorothioate modified nucleotides. The guide strand can also contain 2′F and/or 2′OMe modifications, which can be located throughout the molecule. In some embodiments, the nucleotide in position one of the guide strand (the nucleotide in the most 5′ position of the guide strand) is 2′OMe modified and/or phosphorylated. C and U nucleotides within the guide strand can be 2′F modified. For example, C and U nucleotides in positions 2-10 of a 19 nt guide strand (or corresponding positions in a guide strand of a different length) can be 2′F modified. C and U nucleotides within the guide strand can also be 2′OMe modified. For example, C and U nucleotides in positions 11-18 of a 19 nt guide strand (or corresponding positions in a guide strand of a different length) can be 2′OMe modified. In some embodiments, the nucleotide at the most 3′ end of the guide strand is to unmodified. In certain embodiments, the majority of Cs and Us within the guide strand are 2′F modified and the 5′ end of the guide strand is phosphorylated. In other embodiments, position 1 and the Cs or Us in positions 11-18 are 2′OMe modified and the 5′ end of the guide strand is phosphorylated. In other embodiments, position 1 and the Cs or Us in positions 11-18 are 2′OMe modified, the 5′ end of the guide strand is phosphorylated, and the Cs or Us in position 2-10 are 2′F modified.

In some aspects, an optimal passenger strand is approximately 11-14 nucleotides in length. The passenger strand may contain modifications that confer increased stability. One or more nucleotides in the passenger strand can be 2′OMe modified. In some embodiments, one or more of the C and/or U nucleotides in the passenger strand is 2′OMe modified, or all of the C and U nucleotides in the passenger strand are 2′OMe modified. In certain embodiments, all of the nucleotides in the passenger strand are 2′OMe modified. One or more of the nucleotides on the passenger strand can also be phosphate-modified such as phosphorothioate modified. The passenger strand can also contain 2′ ribo, 2′F and 2 deoxy modifications or any combination of the above. As demonstrated in the Examples, chemical modification patterns on both the guide and passenger strand are well tolerated and a combination of chemical modifications is shown herein to lead to increased efficacy and self-delivery of RNA molecules.

Aspects of the invention relate to RNAi constructs that have extended single-stranded regions relative to double stranded regions, as compared to molecules that have been used previously for RNAi. The single stranded region of the molecules may be modified to promote cellular uptake or gene silencing. In some embodiments, phosphorothioate modification of the single stranded region influences cellular uptake and/or gene silencing. The region of the guide strand that is phosphorothioate modified can include nucleotides within both the single stranded and double stranded regions of the molecule. In some embodiments, the single stranded region includes 2-12 phosphorothioate modifications. For example, the single stranded region can include 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 phosphorothioate modifications. In some instances, the single stranded region contains 6-8 phosphorothioate modifications.

Molecules associated with the invention are also optimized for cellular uptake. In RNA molecules described herein, the guide and/or passenger strands can be attached to a conjugate. In certain embodiments the conjugate is hydrophobic. The hydrophobic conjugate can be a small molecule with a partition coefficient that is higher than 10. The conjugate can be a sterol-type molecule such as cholesterol, or a molecule with an increased length polycarbon chain attached to C17, and the presence of a conjugate can influence the ability of an RNA molecule to be taken into a cell with or without a lipid transfection reagent. The conjugate can be attached to the passenger or guide strand through a hydrophobic linker. In some embodiments, a hydrophobic linker is 5-12C in length, and/or is hydroxypyrrolidine-based. In some embodiments, a hydrophobic conjugate is attached to the passenger strand and the CU residues of either the passenger and/or guide strand are modified. In some embodiments, at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or 95% of the CU residues on the passenger strand and/or the guide strand are modified. In some aspects, molecules associated with the invention are self-delivering (sd). As used herein, “self-delivery” refers to the ability of a molecule to be delivered into a cell without the need for an additional delivery vehicle such as a transfection reagent.

Aspects of the invention relate to selecting molecules for use in RNAi. Based on the data described herein, molecules that have a double stranded region of 8-14 nucleotides can be selected for use in RNAi. In some embodiments, molecules are selected based on their thermodynamic stability (ΔG). In some embodiments, molecules will be selected that have a (ΔG) of less than −13 kkal/mol. For example, the (ΔG) value may be −13, −14, −15, −16, −17, −18, −19, −21, −22 or less than −22 kkal/mol. In other embodiments, the (ΔG) value may be higher than −13 kkal/mol. For example, the (ΔG) value may be −12, −11, −10, −9, −8, −7 or more than −7 kkal/mol. It should be appreciated that ΔG can be calculated using any method known in the art. In some embodiments ΔG is calculated using Mfold, available through the Mfold internet site (http://mfold.bioinfo.rpi.edu/cai-bin/rna-form1.cgi). Methods for calculating ΔG are described in, and are incorporated by reference from, the following references: Zuker, M. (2003) Nucleic Acids Res., 31(13):3406-15; Mathews, D. H., Sabina, J., Zuker, M. and Turner, D. H. (1999) J. Mol. Biol. 288:911-940; Mathews, D. H., Disney, M. D., Childs, J. L., Schroeder, S. J., Zuker, M., and Turner, D. H. (2004) Proc. Natl. Acad. Sci. 101:7287-7292; Duan, S., Mathews, D. H., and Turner, D. H. (2006) Biochemistry 45:9819-9832; Wuchty, S., Fontana, W., Hofacker, 1. L., and Schuster, P. (1999) Biopolymers 49:145-165.

Aspects of the invention relate to using nucleic acid molecules described herein, with minimal double stranded regions and/or with a (ΔG) of less than −13 kkal/mol, for gene silencing. RNAi molecules can be administered in vivo or in vitro, and gene silencing effects can be achieved in vivo or in vitro.

In certain embodiments, the polynucleotide contains 5′- and/or 3′-end overhangs. The number and/or sequence of nucleotides overhang on one end of the polynucleotide may be the same or different from the other end of the polynucleotide. In certain embodiments, one or more of the overhang nucleotides may contain chemical modification(s), such as phosphorothioate or 2′-OMe modification.

In certain embodiments, the polynucleotide is unmodified. In other embodiments, at least one nucleotide is modified. In further embodiments, the modification includes a 2′-H or 2′-modified ribose sugar at the 2nd nucleotide from the 5′-end of the guide sequence. The “2nd nucleotide” is defined as the second nucleotide from the 5′-end of the polynucleotide.

As used herein, “2′-modified ribose sugar” includes those ribose sugars that do not have a 2′-OH group. “2′-modified ribose sugar” does not include 2′-deoxyribose (found in unmodified canonical DNA nucleotides). For example, the 2′-modified ribose sugar may be 2′-O-alkyl nucleotides, 2′-deoxy-2′-fluoro nucleotides, 2′-deoxy nucleotides, or combination thereof.

In certain embodiments, the 2′-modified nucleotides are pyrimidine nucleotides (e.g., C/U). Examples of 2′-O-alkyl nucleotides include 2′-O-methyl nucleotides, or 2′-O-allyl nucleotides.

In certain embodiments, the miniRNA polynucleotide of the invention with the above-referenced 5′-end modification exhibits significantly (e.g., at least about 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or more) less “off-target” gene silencing when compared to similar constructs without the specified 5′-end modification, thus greatly improving the overall specificity of the RNAi reagent or therapeutics.

As used herein, “off-target” gene silencing refers to unintended gene silencing due to, for example, spurious sequence homology between the antisense (guide) sequence and the unintended target mRNA sequence.

According to this aspect of the invention, certain guide strand modifications further increase nuclease stability, and/or lower interferon induction, without significantly decreasing RNAi activity (or no decrease in RNAi activity at all).

In some embodiments, wherein the RNAi construct involves a hairpin, the 5′-stem sequence may comprise a 2′-modified ribose sugar, such as 2′-O-methyl modified nucleotide, at the 2^(nd) nucleotide on the 5′-end of the polynucleotide and, in some embodiments, no other modified nucleotides. The hairpin structure having such modification may have enhanced target specificity or reduced off-target silencing compared to a similar construct without the 2′-O-methyl modification at said position.

Certain combinations of specific 5′-stem sequence and 3′-stem sequence modifications may result in further unexpected advantages, as partly manifested by enhanced ability to inhibit target gene expression, enhanced serum stability, and/or increased target specificity, etc.

In certain embodiments, the guide strand comprises a 2′-O-methyl modified nucleotide at the 2^(nd) nucleotide on the 5′-end of the guide strand and no other modified nucleotides.

In other aspects, the miniRNA structures of the present invention mediates sequence-dependent gene silencing by a microRNA mechanism. As used herein, the term “microRNA” (“miRNA”), also referred to in the art as “small temporal RNAs” (“stRNAs”), refers to a small (10-50 nucleotide) RNA which are genetically encoded (e.g., by viral, mammalian, or plant genomes) and are capable of directing or mediating RNA silencing. An “miRNA disorder” shall refer to a disease or disorder characterized by an aberrant expression or activity of an miRNA.

microRNAs are involved in down-regulating target genes in critical pathways, such as development and cancer, in mice, worms and mammals. Gene silencing through a microRNA mechanism is achieved by specific yet imperfect base-pairing of the miRNA and its target messenger RNA (mRNA). Various mechanisms may be used in microRNA-mediated down-regulation of target mRNA expression.

miRNAs are noncoding RNAs of approximately 22 nucleotides which can regulate gene expression at the post transcriptional or translational level during plant and animal development. One common feature of miRNAs is that they are all excised from an approximately 70 nucleotide precursor RNA stem-loop termed pre-miRNA, probably by Dicer, an RNase III-type enzyme, or a homolog thereof. Naturally-occurring miRNAs are expressed by endogenous genes in vivo and are processed from a hairpin or stem-loop precursor (pre-miRNA or pri-miRNAs) by Dicer or other RNAses. miRNAs can exist transiently in vivo as a double-stranded duplex but only one strand is taken up by the RISC complex to direct gene silencing.

In some embodiments a version of sd-rxRNA compounds, which are effective in cellular uptake and inhibiting of miRNA activity are described. Essentially the compounds are similar to RISC entering version but large strand chemical modification patterns are optimized in the way to block cleavage and act as an effective inhibitor of the RISC action. For example, the compound might be completely or mostly Omethyl modified with the PS content described previously. For these types of compounds the 5′ phosphorilation is not necessary. The presence of double stranded region is preferred as it is promotes cellular uptake and efficient RISC loading.

Another pathway that uses small RNAs as sequence-specific regulators is the RNA interference (RNAi) pathway, which is an evolutionarily conserved response to the presence of double-stranded RNA (dsRNA) in the cell. The dsRNAs are cleaved into ˜20-base pair (bp) duplexes of small-interfering RNAs (siRNAs) by Dicer. These small RNAs get assembled into multiprotein effector complexes called RNA-induced silencing complexes (RISCs). The siRNAs then guide the cleavage of target mRNAs with perfect complementarity.

Some aspects of biogenesis, protein complexes, and function are shared between the siRNA pathway and the miRNA pathway. The subject single-stranded polynucleotides may mimic the dsRNA in the siRNA mechanism, or the microRNA in the miRNA mechanism.

In certain embodiments, the modified RNAi constructs may have improved stability in serum and/or cerebral spinal fluid compared to an unmodified RNAi constructs having the same sequence.

In certain embodiments, the structure of the RNAi construct does not induce interferon response in primary cells, such as mammalian primary cells, including primary cells from human, mouse and other rodents, and other non-human mammals. In certain embodiments, the RNAi construct may also be used to inhibit expression of a target gene in an invertebrate organism.

To further increase the stability of the subject constructs in vivo, the 3′-end of the hairpin structure may be blocked by protective group(s). For example, protective groups such as inverted nucleotides, inverted abasic moieties, or amino-end modified nucleotides may be used. Inverted nucleotides may comprise an inverted deoxynucleotide. Inverted abasic moieties may comprise an inverted deoxyabasic moiety, such as a 3′,3′-linked or 5′,5′-linked deoxyabasic moiety.

The RNAi constructs of the invention are capable of inhibiting the synthesis of any target protein encoded by target gene(s). The invention includes methods to inhibit expression of a target gene either in a cell in vitro, or in vivo. As such, the RNAi constructs of the invention are useful for treating a patient with a disease characterized by the overexpression of a target gene.

The target gene can be endogenous or exogenous (e.g., introduced into a cell by a virus or using recombinant DNA technology) to a cell. Such methods may include introduction of RNA into a cell in an amount sufficient to inhibit expression of the target gene. By way of example, such an RNA molecule may have a guide strand that is complementary to the nucleotide sequence of the target gene, such that the composition inhibits expression of the target gene.

The invention also relates to vectors expressing the subject hairpin constructs, and cells comprising such vectors or the subject hairpin constructs. The cell may be a mammalian cell in vivo or in culture, such as a human cell.

The invention further relates to compositions comprising the subject RNAi constructs, and a pharmaceutically acceptable carrier or diluent.

Another aspect of the invention provides a method for inhibiting the expression of a target gene in a mammalian cell, comprising contacting the mammalian cell with any of the subject RNAi constructs.

The method may be carried out in vitro, ex vivo, or in vivo, in, for example, mammalian cells in culture, such as a human cell in culture.

The target cells (e.g., mammalian cell) may be contacted in the presence of a delivery reagent, such as a lipid (e.g., a cationic lipid) or a liposome.

Another aspect of the invention provides a method for inhibiting the expression of a target gene in a mammalian cell, comprising contacting the mammalian cell with a vector expressing the subject RNAi constructs.

In one aspect of the invention, a longer duplex polynucleotide is provided, including a first polynucleotide that ranges in size from about 16 to about 30 nucleotides; a second polynucleotide that ranges in size from about 26 to about 46 nucleotides, wherein the first polynucleotide (the antisense strand) is complementary to both the second polynucleotide (the sense strand) and a target gene, and wherein both polynucleotides form a duplex and wherein the first polynucleotide contains a single stranded region longer than 6 bases in length and is modified with alternative chemical modification pattern, and/or includes a conjugate moiety that facilitates cellular delivery. In this embodiment, between about 40% to about 90% of the nucleotides of the passenger strand between about 40% to about 90% of the nucleotides of the guide strand, and between about 40% to about 90% of the nucleotides of the single stranded region of the first polynucleotide are chemically modified nucleotides.

In an embodiment, the chemically modified nucleotide in the polynucleotide duplex may be any chemically modified nucleotide known in the art, such as those discussed in detail above. In a particular embodiment, the chemically modified nucleotide is selected from the group consisting of 2′ F modified nucleotides, 2′-O-methyl modified and 2′deoxy nucleotides. In another particular embodiment, the chemically modified nucleotides results from “hydrophobic modifications” of the nucleotide base. In another particular embodiment, the chemically modified nucleotides are phosphorothioates. In an additional particular embodiment, chemically modified nucleotides are combination of phosphorothioates, 2′-O-methyl, 2′deoxy, hydrophobic modifications and phosphorothioates. As these groups of modifications refer to modification of the ribose ring, back bone and nucleotide, it is feasible that some modified nucleotides will carry a combination of all three modification types.

In another embodiment, the chemical modification is not the same across the various regions of the duplex. In a particular embodiment, the first polynucleotide (the passenger strand), has a large number of diverse chemical modifications in various positions. For this polynucleotide up to 90% of nucleotides might be chemically modified and/or have mismatches introduced. In another embodiment, chemical modifications of the first or second polynucleotide include, but not limited to, 5′ position modification of Uridine and Cytosine (4-pyridyl, 2-pyridyl, indolyl, phenyl (C₆H₅OH); tryptophanyl (C8H6N)CH2CH(NH2)CO), isobutyl, butyl, aminobenzyl; phenyl; naphthyl, etc), where the chemical modification might alter base pairing capabilities of a nucleotide. For the guide strand an important feature of this aspect of the invention is the position of the chemical modification relative to the 5′ end of the antisense and sequence. For example, chemical phosphorylation of the 5′ end of the guide strand is usually beneficial for efficacy. O-methyl modifications in the seed region of the sense strand (position 2-7 relative to the 5′ end) are not generally well tolerated, whereas 2′F and deoxy are well tolerated. The mid part of the guide strand and the 3′ end of the guide strand are more permissive in a type of chemical modifications applied. Deoxy modifications are not tolerated at the 3′ end of the guide strand.

A unique feature of this aspect of the invention involves the use of hydrophobic modification on the bases. In one embodiment, the hydrophobic modifications are preferably positioned near the 5′ end of the guide strand, in other embodiments, they localized in the middle of the guides strand, in other embodiment they localized at the 3′ end of the guide strand and yet in another embodiment they are distributed thought the whole length of the polynucleotide. The same type of patterns is applicable to the passenger strand of the duplex.

The other part of the molecule is a single stranded region. The single stranded region is expected to range from 7 to 40 nucleotides.

In one embodiment, the single stranded region of the first polynucleotide contains modifications selected from the group consisting of between 40% and 90% hydrophobic base modifications, between 40%-90% phosphorothioates, between 40%-90% modification of the ribose moiety, and any combination of the preceding.

Efficiency of guide strand (first polynucleotide) loading into the RISC complex might be altered for heavily modified polynucleotides, so in one embodiment, the duplex polynucleotide includes a mismatch between nucleotide 9, 11, 12, 13, or 14 on the guide strand (first polynucleotide) and the opposite nucleotide on the sense strand (second polynucleotide) to promote efficient guide strand loading.

More detailed aspects of the invention are described in the sections below.

Duplex Characteristics

Double-stranded oligonucleotides of the invention may be formed by two separate complementary nucleic acid strands. Duplex formation can occur either inside or outside the cell containing the target gene.

As used herein, the term “duplex” includes the region of the double-stranded nucleic acid molecule(s) that is (are) hydrogen bonded to a complementary sequence. Double-stranded oligonucleotides of the invention may comprise a nucleotide sequence that is sense to a target gene and a complementary sequence that is antisense to the target gene. The sense and antisense nucleotide sequences correspond to the target gene sequence, e.g., are identical or are sufficiently identical to effect target gene inhibition (e.g., are about at least about 98% identical, 96% identical, 94%, 90% identical, 85% identical, or 80% identical) to the target gene sequence.

In certain embodiments, the double-stranded oligonucleotide of the invention is double-stranded over its entire length, i.e., with no overhanging single-stranded sequence at either end of the molecule, i.e., is blunt-ended. In other embodiments, the individual nucleic acid molecules can be of different lengths. In other words, a double-stranded oligonucleotide of the invention is not double-stranded over its entire length. For instance, when two separate nucleic acid molecules are used, one of the molecules, e.g., the first molecule comprising an antisense sequence, can be longer than the second molecule hybridizing thereto (leaving a portion of the molecule single-stranded). Likewise, when a single nucleic acid molecule is used a portion of the molecule at either end can remain single-stranded.

In one embodiment, a double-stranded oligonucleotide of the invention contains mismatches and/or loops or bulges, but is double-stranded over at least about 70% of the length of the oligonucleotide. In another embodiment, a double-stranded oligonucleotide of the invention is double-stranded over at least about 80% of the length of the oligonucleotide. In another embodiment, a double-stranded oligonucleotide of the invention is double-stranded over at least about 90%-95% of the length of the oligonucleotide. In another embodiment, a double-stranded oligonucleotide of the invention is double-stranded over at least about 96%-98% of the length of the oligonucleotide. In certain embodiments, the double-stranded oligonucleotide of the invention contains at least or up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 mismatches.

Modifications

The nucleotides of the invention may be modified at various locations, including the sugar moiety, the phosphodiester linkage, and/or the base.

Sugar moieties include natural, unmodified sugars, e.g., monosaccharide (such as pentose, e.g., ribose, deoxyribose), modified sugars and sugar analogs. In general, possible modifications of nucleomonomers, particularly of a sugar moiety, include, for example, replacement of one or more of the hydroxyl groups with a halogen, a heteroatom, an aliphatic group, or the functionalization of the hydroxyl group as an ether, an amine, a thiol, or the like.

One particularly useful group of modified nucleomonomers are 2′-O-methyl nucleotides. Such 2′-O-methyl nucleotides may be referred to as “methylated,” and the corresponding nucleotides may be made from unmethylated nucleotides followed by alkylation or directly from methylated nucleotide reagents. Modified nucleomonomers may be used in combination with unmodified nucleomonomers. For example, an oligonucleotide of the invention may contain both methylated and unmethylated nucleomonomers.

Some exemplary modified nucleomonomers include sugar- or backbone-modified ribonucleotides. Modified ribonucleotides may contain a non-naturally occurring base (instead of a naturally occurring base), such as uridines or cytidines modified at the 5′-position, e.g., 5′-(2-amino)propyl uridine and 5′-bromo uridine; adenosines and guanosines modified at the 8-position, e.g., 8-bromo guanosine; deaza nucleotides, e.g., 7-deaza-adenosine; and N-alkylated nucleotides, e.g., N6-methyl adenosine. Also, sugar-modified ribonucleotides may have the 2′-OH group replaced by a H, alxoxy (or OR), R or alkyl, halogen, SH, SR, amino (such as NH₂, NHR, NR₂), or CN group, wherein R is lower alkyl, alkenyl, or alkynyl.

Modified ribonucleotides may also have the phosphodiester group connecting to adjacent ribonucleotides replaced by a modified group, e.g., of phosphorothioate group. More generally, the various nucleotide modifications may be combined.

Although the antisense (guide) strand may be substantially identical to at least a portion of the target gene (or genes), at least with respect to the base pairing properties, the sequence need not be perfectly identical to be useful, e.g., to inhibit expression of a target gene's phenotype. Generally, higher homology can be used to compensate for the use of a shorter antisense gene. In some cases, the antisense strand generally will be substantially identical (although in antisense orientation) to the target gene.

The use of 2′-O-methyl modified RNA may also be beneficial in circumstances in which it is desirable to minimize cellular stress responses. RNA having 2′-O-methyl nucleomonomers may not be recognized by cellular machinery that is thought to recognize unmodified RNA. The use of 2′-O-methylated or partially 2′-O-methylated RNA may avoid the interferon response to double-stranded nucleic acids, while maintaining target RNA inhibition. This may be useful, for example, for avoiding the interferon or other cellular stress responses, both in short RNAi (e.g., siRNA) sequences that induce the interferon response, and in longer RNAi sequences that may induce the interferon response.

Overall, modified sugars may include D-ribose, 2′-O-alkyl (including 2′-O-methyl and 2′-O-ethyl), i.e., 2′-alkoxy, 2′-amino, 2′-S-alkyl, 2′-halo (including 2′-fluoro), 2′-methoxyethoxy, 2′-allyloxy (—OCH₂CH═CH₂), 2′-propargyl, 2′-propyl, ethynyl, ethenyl, propenyl, and cyano and the like. In one embodiment, the sugar moiety can be a hexose and incorporated into an oligonucleotide as described (Augustyns, K., et al., Nucl. Acids. Res. 18:4711 (1992)). Exemplary nucleomonomers can be found, e.g., in U.S. Pat. No. 5,849,902, incorporated by reference herein.

The term “alkyl” includes saturated aliphatic groups, including straight-chain alkyl groups (e.g., methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, etc.), branched-chain alkyl groups (isopropyl, tert-butyl, isobutyl, etc.), cycloalkyl (alicyclic) groups (cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl), alkyl substituted cycloalkyl groups, and cycloalkyl substituted alkyl groups. In certain embodiments, a straight chain or branched chain alkyl has 6 or fewer carbon atoms in its backbone (e.g., C₁-C₆ for straight chain, C₃-C₆ for branched chain), and more preferably 4 or fewer. Likewise, preferred cycloalkyls have from 3-8 carbon atoms in their ring structure, and more preferably have 5 or 6 carbons in the ring structure. The term C₁-C₆ includes alkyl groups containing 1 to 6 carbon atoms.

Moreover, unless otherwise specified, the term alkyl includes both “unsubstituted alkyls” and “substituted alkyls,” the latter of which refers to alkyl moieties having independently selected substituents replacing a hydrogen on one or more carbons of the hydrocarbon backbone. Such substituents can include, for example, alkenyl, alkynyl, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkyl amino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety. Cycloalkyls can be further substituted, e.g., with the substituents described above. An “alkylaryl” or an “arylalkyl” moiety is an alkyl substituted with an aryl (e.g., phenylmethyl (benzyl)). The term “alkyl” also includes the side chains of natural and unnatural amino acids. The term “n-alkyl” means a straight chain (i.e., unbranched) unsubstituted alkyl group.

The term “alkenyl” includes unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but that contain at least one double bond. For example, the term “alkenyl” includes straight-chain alkenyl groups (e.g., ethylenyl, propenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, etc.), branched-chain alkenyl groups, cycloalkenyl (alicyclic) groups (cyclopropenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl), alkyl or alkenyl substituted cycloalkenyl groups, and cycloalkyl or cycloalkenyl substituted alkenyl groups. In certain embodiments, a straight chain or branched chain alkenyl group has 6 or fewer carbon atoms in its backbone (e.g., C2-C₆ for straight chain, C₃-C₆ for branched chain). Likewise, cycloalkenyl groups may have from 3-8 carbon atoms in their ring structure, and more preferably have 5 or 6 carbons in the ring structure. The term C₂-C₆ includes alkenyl groups containing 2 to 6 carbon atoms.

Moreover, unless otherwise specified, the term alkenyl includes both “unsubstituted alkenyls” and “substituted alkenyls,” the latter of which refers to alkenyl moieties having independently selected substituents replacing a hydrogen on one or more carbons of the hydrocarbon backbone. Such substituents can include, for example, alkyl groups, alkynyl groups, halogens, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkyl amino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety.

The term “alkynyl” includes unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but which contain at least one triple bond. For example, the term “alkynyl” includes straight-chain alkynyl groups (e.g., ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl, decynyl, etc.), branched-chain alkynyl groups, and cycloalkyl or cycloalkenyl substituted alkynyl groups. In certain embodiments, a straight chain or branched chain alkynyl group has 6 or fewer carbon atoms in its backbone (e.g., C₂-C₆ for straight chain, C₃-C₆ for branched chain). The term C₂-C₆ includes alkynyl groups containing 2 to 6 carbon atoms.

Moreover, unless otherwise specified, the term alkynyl includes both “unsubstituted alkynyls” and “substituted alkynyls,” the latter of which refers to alkynyl moieties having independently selected substituents replacing a hydrogen on one or more carbons of the hydrocarbon backbone. Such substituents can include, for example, alkyl groups, alkynyl groups, halogens, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkyl amino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety.

Unless the number of carbons is otherwise specified, “lower alkyl” as used herein means an alkyl group, as defined above, but having from one to five carbon atoms in its backbone structure. “Lower alkenyl” and “lower alkynyl” have chain lengths of, for example, 2-5 carbon atoms.

The term “alkoxy” includes substituted and unsubstituted alkyl, alkenyl, and alkynyl groups covalently linked to an oxygen atom. Examples of alkoxy groups include methoxy, ethoxy, isopropyloxy, propoxy, butoxy, and pentoxy groups. Examples of substituted alkoxy groups include halogenated alkoxy groups. The alkoxy groups can be substituted with independently selected groups such as alkenyl, alkynyl, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkyl amino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulffiydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfmyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moieties. Examples of halogen substituted alkoxy groups include, but are not limited to, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy, trichloromethoxy, etc.

The term “hydrophobic modifications’ include bases modified in a fashion, where (1) overall hydrophobicity of the base is significantly increases, (2) the base is still capable of forming close to regular Watson-Crick interaction. Some, of the examples of base modifications include but are not limited to 5-position uridine and cytidine modifications like phenyl,

4-pyridyl, 2-pyridyl, indolyl, and isobutyl, phenyl (C6H5OH); tryptophanyl (C8H6N)CH2CH(NH2)CO), Isobutyl, butyl, aminobenzyl; phenyl; naphthyl, For purposes of the present invention, the term “overhang” refers to terminal non-base pairing nucleotide(s) resulting from one strand or region extending beyond the terminus of the complementary strand to which the first strand or region forms a duplex. One or more polynucleotides that are capable of forming a duplex through hydrogen bonding can have overhangs. The overhand length generally doesn't exceed 5 bases in length.

The term “heteroatom” includes atoms of any element other than carbon or hydrogen. Preferred heteroatoms are nitrogen, oxygen, sulfur and phosphorus.

The term “hydroxy” or “hydroxyl” includes groups with an —OH or —O⁻ (with an appropriate counterion).

The term “halogen” includes fluorine, bromine, chlorine, iodine, etc. The term “perhalogenated” generally refers to a moiety wherein all hydrogens are replaced by halogen atoms.

The term “substituted” includes independently selected substituents which can be placed on the moiety and which allow the molecule to perform its intended function. Examples of substituents include alkyl, alkenyl, alkynyl, aryl, (CR′R″)₀₋₃NR′R″, (CR′R″)₀₋₃CN, NO₂, halogen, (CR′R″)₀₋₃C(halogen)₃, (CR′R″)₀₋₃CH(halogen)₂, (CR′R″)₀₋₃CH₂(halogen), (CR′R″)₀₋₃CONR′R″, (CR′R″)₀₋₃S(O)₁₋₂NR′R″, (CR′R″)₀₋₃CHO, (CR′R″)₀₋₃O(CR′R″)₀₋₃H, (CR′R″)₀₋₃S(O)₀₋₂R′, (CR′R″)₀₋₃O(CR′R″)₀₋₃H, (CR′R″)₀₋₃COR′, (CR′R″)₀₋₃CO₂R′, or (CR′R″)₀₋₃OR′ groups; wherein each R′ and R″ are each independently hydrogen, a C₁-C₅ alkyl, C₂-C₅ alkenyl, C₂-C₅ alkynyl, or aryl group, or R′ and R″ taken together are a benzylidene group or a —(CH₂)₂O(CH₂)₂— group.

The term “amine” or “amino” includes compounds or moieties in which a nitrogen atom is covalently bonded to at least one carbon or heteroatom. The term “alkyl amino” includes groups and compounds wherein the nitrogen is bound to at least one additional alkyl group. The term “dialkyl amino” includes groups wherein the nitrogen atom is bound to at least two additional alkyl groups.

The term “ether” includes compounds or moieties which contain an oxygen bonded to two different carbon atoms or heteroatoms. For example, the term includes “alkoxyalkyl,” which refers to an alkyl, alkenyl, or alkynyl group covalently bonded to an oxygen atom which is covalently bonded to another alkyl group.

The term “base” includes the known purine and pyrimidine heterocyclic bases, deazapurines, and analogs (including heterocyclic substituted analogs, e.g., aminoethyoxy phenoxazine), derivatives (e.g., 1-alkyl-, 1-alkenyl-, heteroaromatic- and 1-alkynyl derivatives) and tautomers thereof. Examples of purines include adenine, guanine, inosine, diaminopurine, and xanthine and analogs (e.g., 8-oxo-N⁶-methyladenine or 7-diazaxanthine) and derivatives thereof. Pyrimidines include, for example, thymine, uracil, and cytosine, and their analogs (e.g., 5-methylcytosine, 5-methyluracil, 5-(1-propynyl)uracil, 5-(1-propynyl)cytosine and 4,4-ethanocytosine). Other examples of suitable bases include non-purinyl and non-pyrimidinyl bases such as 2-aminopyridine and triazines.

In a preferred embodiment, the nucleomonomers of an oligonucleotide of the invention are RNA nucleotides. In another preferred embodiment, the nucleomonomers of an oligonucleotide of the invention are modified RNA nucleotides. Thus, the oligonucleotides contain modified RNA nucleotides.

The term “nucleoside” includes bases which are covalently attached to a sugar moiety, preferably ribose or deoxyribose. Examples of preferred nucleosides include ribonucleosides and deoxyribonucleosides. Nucleosides also include bases linked to amino acids or amino acid analogs which may comprise free carboxyl groups, free amino groups, or protecting groups. Suitable protecting groups are well known in the art (see P. G. M. Wuts and T. W. Greene, “Protective Groups in Organic Synthesis”, 2^(nd) Ed., Wiley-Interscience, New York, 1999).

The term “nucleotide” includes nucleosides which further comprise a phosphate group or a phosphate analog.

As used herein, the term “linkage” includes a naturally occurring, unmodified phosphodiester moiety (—O—(PO²⁻)—O—) that covalently couples adjacent nucleomonomers. As used herein, the term “substitute linkage” includes any analog or derivative of the native phosphodiester group that covalently couples adjacent nucleomonomers. Substitute linkages include phosphodiester analogs, e.g., phosphorothioate, phosphorodithioate, and P-ethyoxyphosphodiester, P-ethoxyphosphodiester, P-alkyloxyphosphotriester, methylphosphonate, and nonphosphorus containing linkages, e.g., acetals and amides. Such substitute linkages are known in the art (e.g., Bjergarde et al. 1991. Nucleic Acids Res. 19:5843; Caruthers et al. 1991. Nucleosides Nucleotides. 10:47). In certain embodiments, non-hydrolizable linkages are preferred, such as phosphorothioate linkages.

In certain embodiments, oligonucleotides of the invention comprise hydrophobicly modified nucleotides or “hydrophobic modifications.” As used herein “hydrophobic modifications” refers to bases that are modified such that (1) overall hydrophobicity of the base is significantly increased, and/or (2) the base is still capable of forming close to regular Watson-Crick interaction. Several non-limiting examples of base modifications include 5-position uridine and cytidine modifications such as phenyl, 4-pyridyl, 2-pyridyl, indolyl, and isobutyl, phenyl (C6H5OH); tryptophanyl (C8H6N)CH2CH(NH2)CO), Isobutyl, butyl, aminobenzyl; phenyl; and naphthyl.

In certain embodiments, oligonucleotides of the invention comprise 3′ and 5′ termini (except for circular oligonucleotides). In one embodiment, the 3′ and 5′ termini of an oligonucleotide can be substantially protected from nucleases e.g., by modifying the 3′ or 5′ linkages (e.g., U.S. Pat. No. 5,849,902 and WO 98/13526). For example, oligonucleotides can be made resistant by the inclusion of a “blocking group.” The term “blocking group” as used herein refers to substituents (e.g., other than OH groups) that can be attached to oligonucleotides or nucleomonomers, either as protecting groups or coupling groups for synthesis (e.g., FITC, propyl (CH₂—CH₂—CH₃), glycol (—O—CH₂—CH₂—O—) phosphate (PO₃ ²⁻), hydrogen phosphonate, or phosphoramidite). “Blocking groups” also include “end blocking groups” or “exonuclease blocking groups” which protect the 5′ and 3′ termini of the oligonucleotide, including modified nucleotides and non-nucleotide exonuclease resistant structures.

Exemplary end-blocking groups include cap structures (e.g., a 7-methylguanosine cap), inverted nucleomonomers, e.g., with 3′-3′ or 5′-5′ end inversions (see, e.g., Ortiagao et al. 1992. Antisense Res. Dev. 2:129), methylphosphonate, phosphoramidite, non-nucleotide groups (e.g., non-nucleotide linkers, amino linkers, conjugates) and the like. The 3′ terminal nucleomonomer can comprise a modified sugar moiety. The 3′ terminal nucleomonomer comprises a 3′-O that can optionally be substituted by a blocking group that prevents 3′-exonuclease degradation of the oligonucleotide. For example, the 3′-hydroxyl can be esterified to a nucleotide through a 3′→3′ internucleotide linkage. For example, the alkyloxy radical can be methoxy, ethoxy, or isopropoxy, and preferably, ethoxy. Optionally, the 3′→3′linked nucleotide at the 3′ terminus can be linked by a substitute linkage. To reduce nuclease degradation, the 5′ most 3′→5′ linkage can be a modified linkage, e.g., a phosphorothioate or a P-alkyloxyphosphotriester linkage. Preferably, the two 5′ most 3′→5′ linkages are modified linkages. Optionally, the 5′ terminal hydroxy moiety can be esterified with a phosphorus containing moiety, e.g., phosphate, phosphorothioate, or P-ethoxyphosphate.

Another type of conjugates that can be attached to the end (3′ or 5′ end), the loop region, or any other parts of the miniRNA might include a sterol, sterol type molecule, peptide, small molecule, protein, etc. In some embodiments, a miniRNA may contain more than one conjugates (same or different chemical nature). In some embodiments, the conjugate is cholesterol.

Another way to increase target gene specificity, or to reduce off-target silencing effect, is to introduce a 2′-modification (such as the 2′-O methyl modification) at a position corresponding to the second 5′-end nucleotide of the guide sequence. This allows the positioning of this 2′-modification in the Dicer-resistant hairpin structure, thus enabling one to design better RNAi constructs with less or no off-target silencing.

In one embodiment, a hairpin polynucleotide of the invention can comprise one nucleic acid portion which is DNA and one nucleic acid portion which is RNA. Antisense (guide) sequences of the invention can be “chimeric oligonucleotides” which comprise an RNA-like and a DNA-like region.

The language “RNase H activating region” includes a region of an oligonucleotide, e.g., a chimeric oligonucleotide, that is capable of recruiting RNase H to cleave the target RNA strand to which the oligonucleotide binds. Typically, the RNase activating region contains a minimal core (of at least about 3-5, typically between about 3-12, more typically, between about 5-12, and more preferably between about 5-10 contiguous nucleomonomers) of DNA or DNA-like nucleomonomers. (See, e.g., U.S. Pat. No. 5,849,902). Preferably, the RNase H activating region comprises about nine contiguous deoxyribose containing nucleomonomers.

The language “non-activating region” includes a region of an antisense sequence, e.g., a chimeric oligonucleotide, that does not recruit or activate RNase H. Preferably, a non-activating region does not comprise phosphorothioate DNA. The oligonucleotides of the invention comprise at least one non-activating region. In one embodiment, the non-activating region can be stabilized against nucleases or can provide specificity for the target by being complementary to the target and forming hydrogen bonds with the target nucleic acid molecule, which is to be bound by the oligonucleotide.

In one embodiment, at least a portion of the contiguous polynucleotides are linked by a substitute linkage, e.g., a phosphorothioate linkage.

In certain embodiments, most or all of the nucleotides beyond the guide sequence (2′-modified or not) are linked by phosphorothioate linkages. Such constructs tend to have improved pharmacokinetics due to their higher affinity for serum proteins. The phosphorothioate linkages in the non-guide sequence portion of the polynucleotide generally do not interfere with guide strand activity, once the latter is loaded into RISC.

Antisense (guide) sequences of the present invention may include “morpholino oligonucleotides.” Morpholino oligonucleotides are non-ionic and function by an RNase H-independent mechanism. Each of the 4 genetic bases (Adenine, Cytosine, Guanine, and Thymine/Uracil) of the morpholino oligonucleotides is linked to a 6-membered morpholine ring. Morpholino oligonucleotides are made by joining the 4 different subunit types by, e.g., non-ionic phosphorodiamidate inter-subunit linkages. Morpholino oligonucleotides have many advantages including: complete resistance to nucleases (Antisense & Nucl. Acid Drug Dev. 1996. 6:267); predictable targeting (Biochemica Biophysica Acta. 1999. 1489:141); reliable activity in cells (Antisense & Nucl. Acid Drug Dev. 1997. 7:63); excellent sequence specificity (Antisense & Nucl. Acid Drug Dev. 1997. 7:151); minimal non-antisense activity (Biochemica Biophysica Acta. 1999. 1489:141); and simple osmotic or scrape delivery (Antisense & Nucl. Acid Drug Dev. 1997. 7:291). Morpholino oligonuclcotides are also preferred because of their non-toxicity at high doses. A discussion of the preparation of morpholino oligonucleotides can be found in Antisense & Nucl. Acid Drug Dev. 1997. 7:187.

The chemical modifications described herein are believed, based on the data described herein, to promote single stranded polynucleotide loading into the RISC. Single stranded polynucleotides have been shown to be active in loading into RISC and inducing gene silencing. However, the level of activity for single stranded polynucleotides appears to be 2 to 4 orders of magnitude lower when compared to a duplex polynucleotide.

The present invention provides a description of the chemical modification patterns, which may (a) significantly increase stability of the single stranded polynuclcotide (b) promote efficient loading of the polynucleotide into the RISC complex and (c) improve uptake of the single stranded nucleotide by the cell. FIG. 5 provides some non-limiting examples of the chemical modification patterns which may be beneficial for achieving single stranded polynucleotide efficacy inside the cell. The chemical modification patterns may include combination of ribose, backbone, hydrophobic nucleoside and conjugate type of modifications. In addition, in some of the embodiments, the 5′ end of the single polynucleotide may be chemically phosphorylated.

In yet another embodiment, the present invention provides a description of the chemical modifications patterns, which improve functionality of RISC inhibiting polynucleotides. Single stranded polynucleotides have been shown to inhibit activity of a preloaded RISC complex through the substrate competition mechanism. For these types of molecules, conventionally called antagomers, the activity usually requires high concentration and in vivo delivery is not very effective. The present invention provides a description of the chemical modification patterns, which may (a) significantly increase stability of the single stranded polynucleotide (b) promote efficient recognition of the polynucleotide by the RISC as a substrate and/or (c) improve uptake of the single stranded nucleotide by the cell. FIG. 6 provides some non-limiting examples of the chemical modification patterns that may be beneficial for achieving single stranded polynucleotide efficacy inside the cell. The chemical modification patterns may include combination of ribose, backbone, hydrophobic nucleoside and conjugate type of modifications.

The modifications provided by the present invention are applicable to all polynucleotides. This includes single stranded RISC entering polynucleotides, single stranded RISC inhibiting polynucleotides, conventional duplexed polynucleotides of variable length (15-40 bp), asymmetric duplexed polynucleotides, and the like. Polynucleotides may be modified with wide variety of chemical modification patterns, including 5′ end, ribose, backbone and hydrophobic nucleoside modifications.

Synthesis

Oligonucleotides of the invention can be synthesized by any method known in the art, e.g., using enzymatic synthesis and/or chemical synthesis. The oligonucleotides can be synthesized in vitro (e.g., using enzymatic synthesis and chemical synthesis) or in vivo (using recombinant DNA technology well known in the art).

In a preferred embodiment, chemical synthesis is used for modified polynucleotides. Chemical synthesis of linear oligonucleotides is well known in the art and can be achieved by solution or solid phase techniques. Preferably, synthesis is by solid phase methods. Oligonucleotides can be made by any of several different synthetic procedures including the phosphoramidite, phosphite triester, H-phosphonate, and phosphotriester methods, typically by automated synthesis methods.

Oligonucleotide synthesis protocols are well known in the art and can be found, e.g., in U.S. Pat. No. 5,830,653; WO 98/13526; Stec et al. 1984. J. Am. Chem. Soc. 106:6077; Stec et al. 1985. J. Org. Chem. 50:3908; Stec et al. J. Chromatog. 1985. 326:263; LaPlanche et al. 1986. Nucl. Acid. Res. 1986. 14:9081; Fasman G. D., 1989. Practical Handbook of Biochemistry and Molecular Biology. 1989. CRC Press, Boca Raton, Fla.; Lamone. 1993. Biochem. Soc. Trans. 21:1; U.S. Pat. No. 5,013,830; U.S. Pat. No. 5,214,135; U.S. Pat. No. 5,525,719; Kawasaki et al. 1993. J. Med Chem. 36:831; WO 92/03568; U.S. Pat. No. 5,276,019; and U.S. Pat. No. 5,264,423.

The synthesis method selected can depend on the length of the desired oligonucleotide and such choice is within the skill of the ordinary artisan. For example, the phosphoramidite and phosphite triester method can produce oligonucleotides having 175 or more nucleotides, while the H-phosphonate method works well for oligonucleotides of less than 100 nucleotides. If modified bases are incorporated into the oligonucleotide, and particularly if modified phosphodiester linkages are used, then the synthetic procedures are altered as needed according to known procedures. In this regard, Uhlmann et al. (1990, Chemical Reviews 90:543-584) provide references and outline procedures for making oligonucleotides with modified bases and modified phosphodiester linkages. Other exemplary methods for making oligonucleotides are taught in Sonveaux. 1994. “Protecting Groups in Oligonucleotide Synthesis”; Agrawal. Methods in Molecular Biology 26:1. Exemplary synthesis methods are also taught in “Oligonucleotide Synthesis—A Practical Approach” (Gait, M. J. IRL Press at Oxford University Press. 1984). Moreover, linear oligonucleotides of defined sequence, including some sequences with modified nucleotides, are readily available from several commercial sources.

The oligonucleotides may be purified by polyacrylamide gel electrophoresis, or by any of a number of chromatographic methods, including gel chromatography and high pressure liquid chromatography. To confirm a nucleotide sequence, especially unmodified nucleotide sequences, oligonucleotides may be subjected to DNA sequencing by any of the known procedures, including Maxam and Gilbert sequencing, Sanger sequencing, capillary electrophoresis sequencing, the wandering spot sequencing procedure or by using selective chemical degradation of oligonucleotides bound to Hybond paper. Sequences of short oligonucleotides can also be analyzed by laser desorption mass spectroscopy or by fast atom bombardment (McNeal, et al., 1982, J. Am. Chem. Soc. 104:976; Viari, et al., 1987, Biomed Environ. Mass Spectrom. 14:83; Grotjahn et al., 1982, Nuc. Acid Res. 10:4671). Sequencing methods are also available for RNA oligonucleotides.

The quality of oligonucleotides synthesized can be verified by testing the oligonucleotide by capillary electrophoresis and denaturing strong anion HPLC (SAX-HPLC) using, e.g., the method of Bergot and Egan. 1992. J. Chrom. 599:35.

Other exemplary synthesis techniques are well known in the art (see, e.g., Sambrook et al., Molecular Cloning: a Laboratory Manual, Second Edition (1989); DNA Cloning, Volumes I and II (DN Glover Ed. 1985); Oligonucleotide Synthesis (M J Gait Ed, 1984; Nucleic Acid Hybridisation (B D Hames and S J Higgins eds. 1984); A Practical Guide to Molecular Cloning (1984); or the series, Methods in Enzymology (Academic Press, Inc.)).

In certain embodiments, the subject RNAi constructs or at least portions thereof are transcribed from expression vectors encoding the subject constructs. Any art recognized vectors may be use for this purpose. The transcribed RNAi constructs may be isolated and purified, before desired modifications (such as replacing an unmodified sense strand with a modified one, etc.) are carried out.

Delivery/Carrier Uptake of Oligonucleotides by Cells

Oligonucleotides and oligonucleotide compositions are contacted with (i.e., brought into contact with, also referred to herein as administered or delivered to) and taken up by one or more cells or a cell lysate. The term “cells” includes prokaryotic and eukaryotic cells, preferably vertebrate cells, and, more preferably, mammalian cells. In a preferred embodiment, the oligonucleotide compositions of the invention are contacted with human cells.

Oligonucleotide compositions of the invention can be contacted with cells in vitro, e.g., in a test tube or culture dish, (and may or may not be introduced into a subject) or in vivo, e.g., in a subject such as a mammalian subject. Oligonucleotides are taken up by cells at a slow rate by endocytosis, but endocytosed oligonucleotides are generally sequestered and not available, e.g., for hybridization to a target nucleic acid molecule. In one embodiment, cellular uptake can be facilitated by electroporation or calcium phosphate precipitation. However, these procedures are only useful for in vitro or ex vivo embodiments, are not convenient and, in some cases, are associated with cell toxicity.

In another embodiment, delivery of oligonucleotides into cells can be enhanced by suitable art recognized methods including calcium phosphate, DMSO, glycerol or dextran, electroporation, or by transfection, e.g., using cationic, anionic, or neutral lipid compositions or liposomes using methods known in the art (see e.g., WO 90/14074; WO 91/16024; WO 91/17424; U.S. Pat. No. 4,897,355; Bergan et al. 1993. Nucleic Acids Research. 21:3567). Enhanced delivery of oligonucleotides can also be mediated by the use of vectors (See e.g., Shi, Y. 2003. Trends Genet 2003 Jan. 19:9; Reichhart J M et al. Genesis. 2002. 34(1-2):1604, Yu et al. 2002. Proc. Natl. Acad Sci. USA 99:6047; Sui et al. 2002. Proc. Natl. Acad Sci. USA 99:5515) viruses, polyamine or polycation conjugates using compounds such as polylysine, protamine, or Ni, N12-bis (ethyl) spermine (see, e.g., Bartzatt, R. et al. 1989. Blotechnol. Appl. Blochem. 11:133; Wagner E. et al. 1992. Proc. Natl. Acad. Sci. 88:4255).

In certain embodiments, the miniRNA of the invention may be delivered by using various beta-glucan containing particles, such as those described in US 2005/0281781 A1, WO 2006/007372, and WO 2007/050643 (all incorporated herein by reference). In certain embodiments, the beta-glucan particle is derived from yeast. In certain embodiments, the payload trapping molecule is a polymer, such as those with a molecular weight of at least about 1000 Da, 10,000 Da, 50,000 Da, 100 kDa, 500 kDa, etc. Preferred polymers include (without limitation) cationic polymers, chitosans, or PEI (polyethylenimine), etc.

Such beta-glucan based delivery system may be formulated for oral delivery, where the orally delivered beta-glucan/miniRNA constructs may be engulfed by macrophages or other related phagocytic cells, which may in turn release the miniRNA constructs in selected in vivo sites. Alternatively or in addition, the miniRNA may changes the expression of certain macrophage target genes.

The optimal protocol for uptake of oligonucleotides will depend upon a number of factors, the most crucial being the type of cells that are being used. Other factors that are important in uptake include, but are not limited to, the nature and concentration of the oligonucleotide, the confluence of the cells, the type of culture the cells are in (e.g., a suspension culture or plated) and the type of media in which the cells are grown.

Encapsulating Agents

Encapsulating agents entrap oligonucleotides within vesicles. In another embodiment of the invention, an oligonucleotide may be associated with a carrier or vehicle, e.g., liposomes or micelles, although other carriers could be used, as would be appreciated by one skilled in the art. Liposomes are vesicles made of a lipid bilayer having a structure similar to biological membranes. Such carriers are used to facilitate the cellular uptake or targeting of the oligonucleotide, or improve the oligonucleotides pharmacokinetic or toxicological properties.

For example, the oligonucleotides of the present invention may also be administered encapsulated in liposomes, pharmaceutical compositions wherein the active ingredient is contained either dispersed or variously present in corpuscles consisting of aqueous concentric layers adherent to lipidic layers. The oligonucleotides, depending upon solubility, may be present both in the aqueous layer and in the lipidic layer, or in what is generally termed a liposomic suspension. The hydrophobic layer, generally but not exclusively, comprises phopholipids such as lecithin and sphingomyelin, steroids such as cholesterol, more or less ionic surfactants such as diacetylphosphate, stearylamine, or phosphatidic acid, or other materials of a hydrophobic nature. The diameters of the liposomes generally range from about 15 nm to about 5 microns.

The use of liposomes as drug delivery vehicles offers several advantages. Liposomes increase intracellular stability, increase uptake efficiency and improve biological activity. Liposomes are hollow spherical vesicles composed of lipids arranged in a similar fashion as those lipids which make up the cell membrane. They have an internal aqueous space for entrapping water soluble compounds and range in size from 0.05 to several microns in diameter. Several studies have shown that liposomes can deliver nucleic acids to cells and that the nucleic acids remain biologically active. For example, a lipid delivery vehicle originally designed as a research tool, such as Lipofectin or LIPOFECTAMINE™ 2000, can deliver intact nucleic acid molecules to cells.

Specific advantages of using liposomes include the following: they are non-toxic and biodegradable in composition; they display long circulation half-lives; and recognition molecules can be readily attached to their surface for targeting to tissues. Finally, cost-effective manufacture of liposome-based pharmaceuticals, either in a liquid suspension or lyophilized product, has demonstrated the viability of this technology as an acceptable drug delivery system.

In some aspects, formulations associated with the invention might be selected for a class of naturally occurring or chemically synthesized or modified saturated and unsaturated fatty acid residues. Fatty acids might exist in a form of triglycerides, diglycerides or individual fatty acids. In another embodiment, the use of well-validated mixtures of fatty acids and/or fat emulsions currently used in pharmacology for parenteral nutrition may be utilized.

Liposome based formulations are widely used for oligonucleotide delivery. However, most of commercially available lipid or liposome formulations contain at least one positively charged lipid (cationic lipids). The presence of this positively charged lipid is believed to be essential for obtaining a high degree of oligonucleotide loading and for enhancing liposome fusogenic properties. Several methods have been performed and published to identify optimal positively charged lipid chemistries. However, the commercially available liposome formulations containing cationic lipids are characterized by a high level of toxicity. In vivo limited therapeutic indexes have revealed that liposome formulations containing positive charged lipids are associated with toxicity (i.e. elevation in liver enzymes) at concentrations only slightly higher than concentration required to achieve RNA silencing.

New liposome formulations, lacking the toxicity of the prior art liposomes have been developed according to the invention. These new liposome formulations are neutral fat-based formulations for the efficient delivery of oligonucleotides, and in particular for the delivery of the RNA molecules of the invention. The compositions are referred to as neutral nanotransporters because they enable quantitative oligonucleotide incorporation into non-charged lipids mixtures. The lack of toxic levels of cationic lipids in the neutral nanotransporter compositions of the invention is an important feature.

The neutral nanotransporters compositions enable efficient loading of oligonucleotide into neutral fat formulation. The composition includes an oligonucleotide that is modified in a manner such that the hydrophobicity of the molecule is increased (for example a hydrophobic molecule is attached (covalently or no-covalently) to a hydrophobic molecule on the oligonucleotide terminus or a non-terminal nucleotide, base, sugar, or backbone), the modified oligonucleotide being mixed with a neutral fat formulation (for example containing at least 25% of cholesterol and 25% of DOPC or analogs thereof). A cargo molecule, such as another lipid can also be included in the composition. This composition, where part of the formulation is build into the oligonucleotide itself, enables efficient encapsulation of oligonucleotide in neutral lipid particles.

One of several unexpected observations associated with the invention was that the oligonucleotides of the invention could effectively be incorporated in a lipid mixture that was free of cationic lipids and that such a composition could effectively deliver the therapeutic oligonucleotide to a cell in a manner that it is functional. Another unexpected observation was the high level of activity observed when the fatty mixture is composed of a phosphatidylcholine base fatty acid and a sterol such as a cholesterol. For instance, one preferred formulation of neutral fatty mixture is composed of at least 20% of DOPC or DSPC and at least 20% of sterol such as cholesterol. Even as low as 1:5 lipid to oligonucleotide ratio was shown to be sufficient to get complete encapsulation of the oligonucleotide in a non charged formulation. The prior art demonstrated only a 1-5% oligonucleotide encapsulation with non-charged formulations, which is not sufficient to get to a desired amount of in vivo efficacy. Compared to the prior art using neutral lipids the level of oligonucleotide delivery to a cell was quite unexpected.

Stable particles ranging in size from 50 to 140 nm were formed upon complexing of hydrophobic oligonucleotides with preferred formulations. It is interesting to mention that the formulation by itself typically does not form small particles, but rather, forms agglomerates, which are transformed into stable 50-120 nm particles upon addition of the hydrophobic modified oligonucleotide.

The neutral nanotransporter compositions of the invention include a hydrophobic modified polynucleotide, a neutral fatty mixture, and optionally a cargo molecule. A “hydrophobic modified polynucleotide” as used herein is a polynucleotide of the invention (i.e. sd-rxRNA) that has at least one modification that renders the polynucleotide more hydrophobic than the polynucleotide was prior to modification. The modification may be achieved by attaching (covalently or non-covalently) a hydrophobic molecule to the polynucleotide. In some instances the hydrophobic molecule is or includes a lipophilic group.

The term “lipophilic group” means a group that has a higher affinity for lipids than its affinity for water. Examples of lipophilic groups include, but are not limited to, cholesterol, a cholesteryl or modified cholesteryl residue, adamantine, dihydrotesterone, long chain alkyl, long chain alkenyl, long chain alkynyl, olely-lithocholic, cholenic, oleoyl-cholenic, palmityl, heptadecyl, myrisityl, bile acids, cholic acid or taurocholic acid, deoxycholate, oleyl litocholic acid, oleoyl cholenic acid, glycolipids, phospholipids, sphingolipids, isoprenoids, such as steroids, vitamins, such as vitamin E, fatty acids either saturated or unsaturated, fatty acid esters, such as triglycerides, pyrenes, porphyrines, Texaphyrine, adamantane, acridines, biotin, coumarin, fluorescein, rhodamine, Texas-Red, digoxygenin, dimethoxytrityl, t-butyldimethylsilyl, t-butyldiphenylsilyl, cyanine dyes (e.g. Cy3 or Cy5), Hoechst 33258 dye, psoralen, or to ibuprofen. The cholesterol moiety may be reduced (e.g. as in cholestan) or may be substituted (e.g. by halogen). A combination of different lipophilic groups in one molecule is also possible.

The hydrophobic molecule may be attached at various positions of the polynucleotide. As described above, the hydrophobic molecule may be linked to the terminal residue of the polynucleotide such as the 3′ of 5′-end of the polynucleotide. Alternatively, it may be linked to an internal nucleotide or a nucleotide on a branch of the polynucleotide. The hydrophobic molecule may be attached, for instance to a 2′-position of the nucleotide. The hydrophobic molecule may also be linked to the heterocyclic base, the sugar or the backbone of a nucleotide of the polynucleotide.

The hydrophobic molecule may be connected to the polynucleotide by a linker moiety. Optionally the linker moiety is a non-nucleotidic linker moiety. Non-nucleotidic linkers are e.g. abasic residues (dSpacer), oligoethyleneglycol, such as triethyleneglycol (spacer 9) or hexaethylenegylcol (spacer 18), or alkane-diol, such as butanediol. The spacer units are preferably linked by phosphodiester or phosphorothioate bonds. The linker units may appear just once in the molecule or may be incorporated several times, e.g. via phosphodiester, phosphorothioate, methylphosphonate, or amide linkages.

Typical conjugation protocols involve the synthesis of polynucleotides bearing an aminolinker at one or more positions of the sequence, however, a linker is not required. The amino group is then reacted with the molecule being conjugated using appropriate coupling or activating reagents. The conjugation reaction may be performed either with the polynucleotide still bound to a solid support or following cleavage of the polynucleotide in solution phase. Purification of the modified polynucleotide by HPLC typically results in a pure material.

In some embodiments the hydrophobic molecule is a sterol type conjugate, a PhytoSterol conjugate, cholesterol conjugate, sterol type conjugate with altered side chain length, fatty acid conjugate, any other hydrophobic group conjugate, and/or hydrophobic modifications of the internal nucleoside, which provide sufficient hydrophobicity to be incorporated into micelles.

For purposes of the present invention, the term “sterols”, refers or steroid alcohols are a subgroup of steroids with a hydroxyl group at the 3-position of the A-ring. They are amphipathic lipids synthesized from acetyl-coenzyme A via the HMG-CoA reductase pathway. The overall molecule is quite flat. The hydroxyl group on the A ring is polar. The rest of the aliphatic chain is non-polar. Usually sterols are considered to have an 8 carbon chain at position 17.

For purposes of the present invention, the term “sterol type molecules”, refers to steroid alcohols, which are similar in structure to sterols. The main difference is the structure of the ring and number of carbons in a position 21 attached side chain.

For purposes of the present invention, the term “PhytoSterols” (also called plant sterols) are a group of steroid alcohols, phytochemicals naturally occurring in plants. There are more then 200 different known PhytoSterols

For purposes of the present invention, the term “Sterol side chain” refers to a chemical composition of a side chain attached at the position 17 of sterol-type molecule. In a standard definition sterols are limited to a 4 ring structure carrying a 8 carbon chain at position 17. In this invention, the sterol type molecules with side chain longer and shorter than conventional are described. The side chain may branched or contain double back bones.

Thus, sterols useful in the invention, for example, include cholesterols, as well as unique sterols in which position 17 has attached side chain of 2-7 or longer then 9 carbons. In a particular embodiment, the length of the polycarbon tail is varied between 5 and 9 carbons. FIG. 9 demonstrates that there is a correlation between plasma clearance, liver uptake and the length of the polycarbon chain. Such conjugates may have significantly better in vivo efficacy, in particular delivery to liver. These types of molecules are expected to work at concentrations 5 to 9 fold lower then oligonucleotides conjugated to conventional cholesterols.

Alternatively the polynucleotide may be bound to a protein, peptide or positively charged chemical that functions as the hydrophobic molecule. The proteins may be selected from the group consisting of protamine, dsRNA binding domain, and arginine rich peptides. Exemplary positively charged chemicals include spermine, spermidine, cadaverine, and putrescine.

In another embodiment hydrophobic molecule conjugates may demonstrate even higher efficacy when it is combined with optimal chemical modification patterns of the polynucleotide (as described herein in detail), containing but not limited to hydrophobic modifications, phosphorothioate modifications, and 2′ ribo modifications.

In another embodiment the sterol type molecule may be a naturally occurring PhytoSterols such as those shown in FIG. 8. The polycarbon chain may be longer than 9 and may be linear, branched and/or contain double bonds. Some PhytoSterol containing polynucleotide conjugates may be significantly more potent and active in delivery of polynucleotides to various tissues. Some PhytoSterols may demonstrate tissue preference and thus be used as a way to delivery RNAi specifically to particular tissues.

The hydrophobic modified polynucleotide is mixed with a neutral fatty mixture to form a micelle. The neutral fatty acid mixture is a mixture of fats that has a net neutral or slightly net negative charge at or around physiological pH that can form a micelle with the hydrophobic modified polynucleotide. For purposes of the present invention, the term “micelle” refers to a small nanoparticle formed by a mixture of non charged fatty acids and phospholipids. The neutral fatty mixture may include cationic lipids as long as they are present in an amount that does not cause toxicity. In preferred embodiments the neutral fatty mixture is free of cationic lipids. A mixture that is free of cationic lipids is one that has less than 1% and preferably 0% of the total lipid being cationic lipid. The term “cationic lipid” includes lipids and synthetic lipids having a net positive charge at or around physiological pH. The term “anionic lipid” includes lipids and synthetic lipids having a net negative charge at or around physiological pH.

The neutral fats bind to the oligonucleotides of the invention by a strong but non-covalent attraction (e.g., an electrostatic, van der Waals, pi-stacking, etc. interaction).

The neutral fat mixture may include formulations selected from a class of naturally occurring or chemically synthesized or modified saturated and unsaturated fatty acid residues. Fatty acids might exist in a form of triglycerides, diglycerides or individual fatty acids. In another embodiment the use of well-validated mixtures of fatty acids and/or fat emulsions currently used in pharmacology for parenteral nutrition may be utilized.

The neutral fatty mixture is preferably a mixture of a choline based fatty acid and a sterol. Choline based fatty acids include for instance, synthetic phosphocholine derivatives such as DDPC, DLPC, DMPC, DPPC, DSPC, DOPC, POPC, and DEPC. DOPC (chemical registry number 4235-95-4) is dioleoylphosphatidylcholine (also known as dielaidoylphosphatidylcholine, dioleoyl-PC, dioleoylphosphocholine, dioleoyl-sn-glycero-3-phosphocholine, dioleylphosphatidylcholine). DSPC (chemical registry number 816-94-4) is distearoylphosphatidylcholine (also known as 1,2-Distearoyl-sn-Glycero-3-phosphocholine).

The sterol in the neutral fatty mixture may be for instance cholesterol. The neutral fatty mixture may be made up completely of a choline based fatty acid and a sterol or it may optionally include a cargo molecule. For instance, the neutral fatty mixture may have at least 20% or 25% fatty acid and 20% or 25% sterol.

For purposes of the present invention, the term “Fatty acids” relates to conventional description of fatty acid. They may exist as individual entities or in a form of two- and triglycerides. For purposes of the present invention, the term “fat emulsions” refers to safe fat formulations given intravenously to subjects who are unable to get enough fat in their diet. It is an emulsion of soy bean oil (or other naturally occurring oils) and egg phospholipids. Fat emulsions are being used for formulation of some insoluble anesthetics. In this disclosure, fat emulsions might be part of commercially available preparations like Intralipid, Liposyn, Nutrilipid, modified commercial preparations, where they are enriched with particular fatty acids or fully de novo-formulated combinations of fatty acids and phospholipids.

In one embodiment, the cells to be contacted with an oligonucleotide composition of the invention are contacted with a mixture comprising the oligonucleotide and a mixture comprising a lipid, e.g., one of the lipids or lipid compositions described supra for between about 12 hours to about 24 hours. In another embodiment, the cells to be contacted with an oligonucleotide composition are contacted with a mixture comprising the oligonucleotide and a mixture comprising a lipid, e.g., one of the lipids or lipid compositions described supra for between about 1 and about five days. In one embodiment, the cells are contacted with a mixture comprising a lipid and the oligonucleotide for between about three days to as long as about 30 days. In another embodiment, a mixture comprising a lipid is left in contact with the cells for at least about five to about 20 days. In another embodiment, a mixture comprising a lipid is left in contact with the cells for at least about seven to about 15 days.

50%-60% of the formulation can optionally be any other lipid or molecule. Such a lipid or molecule is referred to herein as a cargo lipid or cargo molecule. Cargo molecules include but are not limited to intralipid, small molecules, fusogenic peptides or lipids or other small molecules might be added to alter cellular uptake, endosomal release or tissue distribution properties. The ability to tolerate cargo molecules is important for modulation of properties of these particles, if such properties are desirable. For instance the presence of some tissue specific metabolites might drastically alter tissue distribution profiles. For example use of Intralipid type formulation enriched in shorter or longer fatty chains with various degrees of saturation affects tissue distribution profiles of these type of formulations (and their loads).

An example of a cargo lipid useful according to the invention is a fusogenic lipid. For instance, the zwiterionic lipid DOPE (chemical registry number 4004-5-1, 1,2-Dioleoyl-sn-Glycero-3-phosphoethanolamine) is a preferred cargo lipid.

Intralipid may be comprised of the following composition: 1 000 mL contain: purified soybean oil 90 g, purified egg phospholipids 12 g, glycerol anhydrous 22 g, water for injection q.s. ad 1 000 mL. pH is adjusted with sodium hydroxide to pH approximately 8. Energy content/L: 4.6 MJ (190 kcal). Osmolality (approx.): 300 mOsm/kg water. In another embodiment fat emulsion is Liposyn that contains 5% safflower oil, 5% soybean oil, up to 1.2% egg phosphatides added as an emulsifier and 2.5% glycerin in water for injection. It may also contain sodium hydroxide for pH adjustment. pH 8.0 (6.0-9.0). Liposyn has an osmolarity of 276 m Osmol/liter (actual).

Variation in the identity, amounts and ratios of cargo lipids affects the cellular uptake and tissue distribution characteristics of these compounds. For example, the length of lipid tails and level of saturability will affect differential uptake to liver, lung, fat and cardiomyocytes. Addition of special hydrophobic molecules like vitamins or different forms of sterols can favor distribution to special tissues which are involved in the metabolism of particular compounds. Complexes are formed at different oligonucleotide concentrations, with higher concentrations favoring more efficient complex formation (FIGS. 21-22).

In another embodiment, the fat emulsion is based on a mixture of lipids. Such lipids may include natural compounds, chemically synthesized compounds, purified fatty acids or any other lipids. In yet another embodiment the composition of fat emulsion is entirely artificial. In a particular embodiment, the fat emulsion is more then 70% linoleic acid. In yet another particular embodiment the fat emulsion is at least 1% of cardiolipin. Linoleic acid (LA) is an unsaturated omega-6 fatty acid. It is a colorless liquid made of a carboxylic acid with an 18-carbon chain and two cis double bonds.

In yet another embodiment of the present invention, the alteration of the composition of the fat emulsion is used as a way to alter tissue distribution of hydrophobicly modified polynucleotides. This methodology provides for the specific delivery of the polynucleotides to particular tissues (FIG. 12).

In another embodiment the fat emulsions of the cargo molecule contain more then 70% of Linoleic acid (C18H3202) and/or cardiolipin are used for specifically delivering RNAi to heart muscle.

Fat emulsions, like intralipid have been used before as a delivery formulation for some non-water soluble drugs (such as Propofol, re-formulated as Diprivan). Unique features of the present invention include (a) the concept of combining modified polynucleotides with the hydrophobic compound(s), so it can be incorporated in the fat micelles and (b) mixing it with the fat emulsions to provide a reversible carrier. After injection into a blood stream, micelles usually bind to serum proteins, including albumin, HDL, LDL and other. This binding is reversible and eventually the fat is absorbed by cells. The polynucleotide, incorporated as a part of the micelle will then be delivered closely to the surface of the cells. After that cellular uptake might be happening though variable mechanisms, including but not limited to sterol type delivery.

Complexing Agents

Complexing agents bind to the oligonucleotides of the invention by a strong but non-covalent attraction (e.g., an electrostatic, van der Waals, pi-stacking, etc. interaction). In one embodiment, oligonucleotides of the invention can be complexed with a complexing agent to increase cellular uptake of oligonucleotides. An example of a complexing agent includes cationic lipids. Cationic lipids can be used to deliver oligonucleotides to cells. However, as discussed above, formulations free in cationic lipids are preferred in some embodiments.

The term “cationic lipid” includes lipids and synthetic lipids having both polar and non-polar domains and which are capable of being positively charged at or around physiological pH and which bind to polyanions, such as nucleic acids, and facilitate the delivery of nucleic acids into cells. In general cationic lipids include saturated and unsaturated alkyl and alicyclic ethers and esters of amines, amides, or derivatives thereof. Straight-chain and branched alkyl and alkenyl groups of cationic lipids can contain, e.g., from 1 to about 25 carbon atoms. Preferred straight chain or branched alkyl or alkene groups have six or more carbon atoms. Alicyclic groups include cholesterol and other steroid groups. Cationic lipids can be prepared with a variety of counterions (anions) including, e.g., Cl⁻, Br⁻, I⁻, F⁻, acetate, trifluoroacetate, sulfate, nitrite, and nitrate.

Examples of cationic lipids include polyethylenimine, polyamidoamine (PAMAM) starburst dendrimers, Lipofectin (a combination of DOTMA and DOPE), Lipofectase, LIPOFECTAMINE™ (e.g., LIPOFECTAMINE™ 2000), DOPE, Cytofectin (Gilead Sciences, Foster City, Calif.), and Eufectins (JBL, San Luis Obispo, Calif.). Exemplary cationic liposomes can be made from N-[1-(2,3-dioleoloxy)-propyl]-N,N,N-trimethylammonium chloride (DOTMA), N-[1-(2,3-dioleoloxy)-propyl]-N,N,N-trimethylammonium methylsulfate (DOTAP), 3β-[N—(N′,N′-dimethylaminoethane)carbamoyl]cholesterol (DC-Chol), 2,3,-dioleyloxy-N-[2(sperminecarboxamido)ethyl]-N,N-dimethyl-1-propanaminium trifluoroacetate (DOSPA), 1,2-dimyristyloxypropyl-3-dimethyl-hydroxyethyl ammonium bromide; and dimethyldioctadecylammonium bromide (DDAB). The cationic lipid N-(1-(2,3-dioleyloxy)propyl)-N,N,N-trimethylammonium chloride (DOTMA), for example, was found to increase 1000-fold the antisense effect of a phosphorothioate oligonucleotide. (Vlassov et al., 1994, Biochimica et Biophysica Acta 1197:95-108). Oligonucleotides can also be complexed with, e.g., poly (L-lysine) or avidin and lipids may, or may not, be included in this mixture, e.g., steryl-poly (L-lysine).

Cationic lipids have been used in the art to deliver oligonucleotides to cells (see, e.g., U.S. Pat. Nos. 5,855,910; 5,851,548; 5,830,430; 5,780,053; 5,767,099; Lewis et al. 1996. Proc. Natl. Acad. Sci. USA 93:3176; Hope et al. 1998. Molecular Membrane Biology 15:1). Other lipid compositions which can be used to facilitate uptake of the instant oligonucleotides can be used in connection with the claimed methods. In addition to those listed supra, other lipid compositions are also known in the art and include, e.g., those taught in U.S. Pat. No. 4,235,871; U.S. Pat. Nos. 4,501,728; 4,837,028; 4,737,323.

In one embodiment lipid compositions can further comprise agents, e.g., viral proteins to enhance lipid-mediated transfections of oligonucleotides (Kamata, et al., 1994. Nucl. Acids. Res. 22:536). In another embodiment, oligonucleotides are contacted with cells as part of a composition comprising an oligonucleotide, a peptide, and a lipid as taught, e.g., in U.S. Pat. No. 5,736,392. Improved lipids have also been described which are serum resistant (Lewis, et al., 1996. Proc. Natl. Acad Sci. 93:3176). Cationic lipids and other complexing agents act to increase the number of oligonucleotides carried into the cell through endocytosis.

In another embodiment N-substituted glycine oligonucleotides (peptoids) can be used to optimize uptake of oligonucleotides. Peptoids have been used to create cationic lipid-like compounds for transfection (Murphy, et al., 1998. Proc. Natl. Acad Sci. 95:1517). Peptoids can be synthesized using standard methods (e.g., Zuckermann, R. N., et al. 1992. J. Am. Chem. Soc. 114:10646; Zuckermann, R. N., et al. 1992. Int. J. Peptide Protein Res. 40:497). Combinations of cationic lipids and peptoids, liptoids, can also be used to optimize uptake of the subject oligonucleotides (Hunag, et al., 1998. Chemistry and Biology. 5:345). Liptoids can be synthesized by elaborating peptoid oligonucleotides and coupling the amino terminal submonomer to a lipid via its amino group (Hunag, et al., 1998. Chemistry and Biology. 5:345).

It is known in the art that positively charged amino acids can be used for creating highly active cationic lipids (Lewis et al. 1996. Proc. Natl. Acad. Sci. USA. 93:3176). In one embodiment, a composition for delivering oligonucleotides of the invention comprises a number of arginine, lysine, histidine or ornithine residues linked to a lipophilic moiety (see e.g., U.S. Pat. No. 5,777,153).

In another embodiment, a composition for delivering oligonucleotides of the invention comprises a peptide having from between about one to about four basic residues. These basic residues can be located, e.g., on the amino terminal, C-terminal, or internal region of the peptide. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine (can also be considered non-polar), asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalaninc, methionine, tryptophan), beta-branched side chains (e.g., threoninc, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Apart from the basic amino acids, a majority or all of the other residues of the peptide can be selected from the non-basic amino acids, e.g., amino acids other than lysine, arginine, or histidine. Preferably a preponderance of neutral amino acids with long neutral side chains are used.

In one embodiment, a composition for delivering oligonucleotides of the invention comprises a natural or synthetic polypeptide having one or more gamma carboxyglutamic acid residues, or γ-Gla residues. These gamma carboxyglutamic acid residues may enable the polypeptide to bind to each other and to membrane surfaces. In other words, a polypeptide having a series of γ-Gla may be used as a general delivery modality that helps an RNAi construct to stick to whatever membrane to which it comes in contact. This may at least slow RNAi constructs from being cleared from the blood stream and enhance their chance of homing to the target.

The gamma carboxyglutamic acid residues may exist in natural proteins (for example, prothrombin has 10 γ-Gla residues). Alternatively, they can be introduced into the purified, recombinantly produced, or chemically synthesized polypeptides by carboxylation using, for example, a vitamin K-dependent carboxylase. The gamma carboxyglutamic acid residues may be consecutive or non-consecutive, and the total number and location of such gamma carboxyglutamic acid residues in the polypeptide can be regulated/fine tuned to achieve different levels of “stickiness” of the polypeptide.

In one embodiment, the cells to be contacted with an oligonucleotide composition of the invention are contacted with a mixture comprising the oligonucleotide and a mixture comprising a lipid, e.g., one of the lipids or lipid compositions described supra for between about 12 hours to about 24 hours. In another embodiment, the cells to be contacted with an oligonucleotide composition are contacted with a mixture comprising the oligonucleotide and a mixture comprising a lipid, e.g., one of the lipids or lipid compositions described supra for between about 1 and about five days. In one embodiment, the cells are contacted with a mixture comprising a lipid and the oligonucleotide for between about three days to as long as about 30 days. In another embodiment, a mixture comprising a lipid is left in contact with the cells for at least about five to about 20 days. In another embodiment, a mixture comprising a lipid is left in contact with the cells for at least about seven to about 15 days.

For example, in one embodiment, an oligonucleotide composition can be contacted with cells in the presence of a lipid such as cytofectin CS or GSV (available from Glen Research; Sterling, Va.), GS3815, GS2888 for prolonged incubation periods as described herein.

In one embodiment, the incubation of the cells with the mixture comprising a lipid and an oligonucleotide composition does not reduce the viability of the cells. Preferably, after the transfection period the cells are substantially viable. In one embodiment, after transfection, the cells are between at least about 70% and at least about 100% viable. In another embodiment, the cells are between at least about 80% and at least about 95% viable. In yet another embodiment, the cells are between at least about 85% and at least about 90% viable.

In one embodiment, oligonucleotides are modified by attaching a peptide sequence that transports the oligonucleotide into a cell, referred to herein as a “transporting peptide.” In one embodiment, the composition includes an oligonucleotide which is complementary to a target nucleic acid molecule encoding the protein, and a covalently attached transporting peptide.

The language “transporting peptide” includes an amino acid sequence that facilitates the transport of an oligonucleotide into a cell. Exemplary peptides which facilitate the transport of the moieties to which they are linked into cells are known in the art, and include, e.g., HIV TAT transcription factor, lactoferrin, Herpes VP22 protein, and fibroblast growth factor 2 (Pooga et al. 1998. Nature Biotechnology. 16:857; and Derossi et al. 1998. Trends in Cell Biology. 8:84; Elliott and O'Hare. 1997. Cell 88:223).

Oligonucleotides can be attached to the transporting peptide using known techniques, e.g., (Prochiantz, A. 1996. Curr. Opin. Neurobiol. 6:629; Derossi et al. 1998. Trends Cell Biol. 8:84; Troy et al. 1996. J. Neurosci. 16:253), Vives et al. 1997. J. Biol. Chem. 272:16010). For example, in one embodiment, oligonucleotides bearing an activated thiol group are linked via that thiol group to a cysteine present in a transport peptide (e.g., to the cysteine present in the β turn between the second and the third helix of the antennapedia homeodomain as taught, e.g., in Derossi et al. 1998. Trends Cell Biol. 8:84; Prochiantz. 1996. Current Opinion in Neurobiol. 6:629; Allinquant et al. 1995. J Cell Biol. 128:919). In another embodiment, a Boc-Cys-(Npys)OH group can be coupled to the transport peptide as the last (N-terminal) amino acid and an oligonucleotide bearing an SH group can be coupled to the peptide (Troy et al. 1996. J. Neurosci. 16:253).

In one embodiment, a linking group can be attached to a nucleomonomer and the transporting peptide can be covalently attached to the linker. In one embodiment, a linker can function as both an attachment site for a transporting peptide and can provide stability against nucleases. Examples of suitable linkers include substituted or unsubstituted C₁-C₂₀ alkyl chains, C₂-C₂₀ alkenyl chains, C₂-C₂₀ alkynyl chains, peptides, and heteroatoms (e.g., S, O, NH, etc.). Other exemplary linkers include bifunctional crosslinking agents such as sulfosuccinimidyl-4-(maleimidophenyl)-butyrate (SMPB) (see, e.g., Smith et al. Biochem J 1991. 276: 417-2).

In one embodiment, oligonucleotides of the invention are synthesized as molecular conjugates which utilize receptor-mediated endocytotic mechanisms for delivering genes into cells (see, e.g., Bunnell et al. 1992. Somatic Cell and Molecular Genetics. 18:559, and the references cited therein).

Targeting Agents

The delivery of oligonucleotides can also be improved by targeting the oligonucleotides to a cellular receptor. The targeting moieties can be conjugated to the oligonucleotides or attached to a carrier group (i.e., poly(L-lysine) or liposomes) linked to the oligonucleotides. This method is well suited to cells that display specific receptor-mediated endocytosis.

For instance, oligonucleotide conjugates to 6-phosphomannosylated proteins are internalized 20-fold more efficiently by cells expressing mannose 6-phosphate specific receptors than free oligonucleotides. The oligonucleotides may also be coupled to a ligand for a cellular receptor using a biodegradable linker. In another example, the delivery construct is mannosylated streptavidin which forms a tight complex with biotinylated oligonucleotides. Mannosylated streptavidin was found to increase 20-fold the internalization of biotinylated oligonucleotides. (Vlassov et al. 1994. Biochimica et Biophysica Acta 1197:95-108).

In addition specific ligands can be conjugated to the polylysine component of polylysine-based delivery systems. For example, transferrin-polylysine, adenovirus-polylysine, and influenza virus hemagglutinin HA-2 N-terminal fusogenic peptides-polylysine conjugates greatly enhance receptor-mediated DNA delivery in eucaryotic cells. Mannosylated glycoprotein conjugated to poly(L-lysine) in aveolar macrophages has been employed to enhance the cellular uptake of oligonucleotides. Liang et al. 1999. Pharmazie 54:559-566.

Because malignant cells have an increased need for essential nutrients such as folic acid and transferrin, these nutrients can be used to target oligonucleotides to cancerous cells. For example, when folic acid is linked to poly(L-lysine) enhanced oligonucleotide uptake is seen in promyelocytic leukaemia (HL-60) cells and human melanoma (M-14) cells. Ginobbi et al. 1997. Anticancer Res. 17:29. In another example, liposomes coated with maleylated bovine serum albumin, folic acid, or ferric protoporphyrin IX, show enhanced cellular uptake of oligonucleotides in murine macrophages, KB cells, and 2.2.15 human hepatoma cells. Liang et al. 1999. Pharmazie 54:559-566.

Liposomes naturally accumulate in the liver, spleen, and reticuloendothelial system (so-called, passive targeting). By coupling liposomes to various ligands such as antibodies are protein A, they can be actively targeted to specific cell populations. For example, protein A-bearing liposomes may be pretreated with H-2K specific antibodies which are targeted to the mouse major histocompatibility complex-encoded H-2K protein expressed on L cells. (Vlassov et al. 1994. Biochimica et Biophysica Acta 1197:95-108).

Other in vitro and/or in vivo delivery of RNAi reagents are known in the art, and can be used to deliver the subject RNAi constructs. See, for example, U.S. patent application publications 20080152661, 20080112916, 20080107694, 20080038296, 20070231392, 20060240093, 20060178327, 20060008910, 20050265957, 20050064595, 20050042227, 20050037496, 20050026286, 20040162235, 20040072785, 20040063654, 20030157030, WO 2008/036825, WO04/065601, and AU2004206255B2, just to name a few (all incorporated by reference).

Administration

The optimal course of administration or delivery of the oligonucleotides may vary depending upon the desired result and/or on the subject to be treated. As used herein “administration” refers to contacting cells with oligonucleotides and can be performed in vitro or in vivo. The dosage of oligonucleotides may be adjusted to optimally reduce expression of a protein translated from a target nucleic acid molecule, e.g., as measured by a readout of RNA stability or by a therapeutic response, without undue experimentation.

For example, expression of the protein encoded by the nucleic acid target can be measured to determine whether or not the dosage regimen needs to be adjusted accordingly. In addition, an increase or decrease in RNA or protein levels in a cell or produced by a cell can be measured using any art recognized technique. By determining whether transcription has been decreased, the effectiveness of the oligonucleotide in inducing the cleavage of a target RNA can be determined.

Any of the above-described oligonucleotide compositions can be used alone or in conjunction with a pharmaceutically acceptable carrier. As used herein, “pharmaceutically acceptable carrier” includes appropriate solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like. The use of such media and agents for pharmaceutical active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, it can be used in the therapeutic compositions. Supplementary active ingredients can also be incorporated into the compositions.

Oligonucleotides may be incorporated into liposomes or liposomes modified with polyethylene glycol or admixed with cationic lipids for parenteral administration. Incorporation of additional substances into the liposome, for example, antibodies reactive against membrane proteins found on specific target cells, can help target the oligonucleotides to specific cell types.

Moreover, the present invention provides for administering the subject oligonucleotides with an osmotic pump providing continuous infusion of such oligonucleotides, for example, as described in Rataiczak et al. (1992 Proc. Natl. Acad. Sci. USA 89:11823-11827). Such osmotic pumps are commercially available, e.g., from Alzet Inc. (Palo Alto, Calif.). Topical administration and parenteral administration in a cationic lipid carrier are preferred.

With respect to in vivo applications, the formulations of the present invention can be administered to a patient in a variety of forms adapted to the chosen route of administration, e.g., parenterally, orally, or intraperitoneally. Parenteral administration, which is preferred, includes administration by the following routes: intravenous; intramuscular; interstitially; intraarterially; subcutaneous; intra ocular; intrasynovial; trans epithelial, including transdermal; pulmonary via inhalation; ophthalmic; sublingual and buccal; topically, including ophthalmic; dermal; ocular; rectal; and nasal inhalation via insufflation.

Pharmaceutical preparations for parenteral administration include aqueous solutions of the active compounds in water-soluble or water-dispersible form. In addition, suspensions of the active compounds as appropriate oily injection suspensions may be administered. Suitable lipophilic solvents or vehicles include fatty oils, for example, sesame oil, or synthetic fatty acid esters, for example, ethyl oleate or triglycerides. Aqueous injection suspensions may contain substances which increase the viscosity of the suspension include, for example, sodium carboxymethyl cellulose, sorbitol, or dextran, optionally, the suspension may also contain stabilizers. The oligonucleotides of the invention can be formulated in liquid solutions, preferably in physiologically compatible buffers such as Hank's solution or Ringer's solution. In addition, the oligonucleotides may be formulated in solid form and redissolved or suspended immediately prior to use. Lyophilized forms are also included in the invention.

Pharmaceutical preparations for topical administration include transdermal patches, ointments, lotions, creams, gels, drops, sprays, suppositories, liquids and powders. In addition, conventional pharmaceutical carriers, aqueous, powder or oily bases, or thickeners may be used in pharmaceutical preparations for topical administration.

Pharmaceutical preparations for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets or tablets. In addition, thickeners, flavoring agents, diluents, emulsifiers, dispersing aids, or binders may be used in pharmaceutical preparations for oral administration.

For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are known in the art, and include, for example, for transmucosal administration bile salts and fusidic acid derivatives, and detergents. Transmucosal administration may be through nasal sprays or using suppositories. For oral administration, the oligonucleotides are formulated into conventional oral administration forms such as capsules, tablets, and tonics. For topical administration, the oligonucleotides of the invention are formulated into ointments, salves, gels, or creams as known in the art.

Drug delivery vehicles can be chosen e.g., for in vitro, for systemic, or for topical administration. These vehicles can be designed to serve as a slow release reservoir or to deliver their contents directly to the target cell. An advantage of using some direct delivery drug vehicles is that multiple molecules are delivered per uptake. Such vehicles have been shown to increase the circulation half-life of drugs that would otherwise be rapidly cleared from the blood stream. Some examples of such specialized drug delivery vehicles which fall into this category are liposomes, hydrogels, cyclodextrins, biodegradable nanocapsules, and bioadhesive microspheres.

The described oligonucleotides may be administered systemically to a subject. Systemic absorption refers to the entry of drugs into the blood stream followed by distribution throughout the entire body. Administration routes which lead to systemic absorption include: intravenous, subcutaneous, intraperitoneal, and intranasal. Each of these administration routes delivers the oligonucleotide to accessible diseased cells. Following subcutaneous administration, the therapeutic agent drains into local lymph nodes and proceeds through the lymphatic network into the circulation. The rate of entry into the circulation has been shown to be a function of molecular weight or size. The use of a liposome or other drug carrier localizes the oligonucleotide at the lymph node. The oligonucleotide can be modified to diffuse into the cell, or the liposome can directly participate in the delivery of either the unmodified or modified oligonucleotide into the cell.

The chosen method of delivery will result in entry into cells. Preferred delivery methods include liposomes (10-400 nm), hydrogels, controlled-release polymers, and other pharmaceutically applicable vehicles, and microinjection or electroporation (for ex vivo treatments).

The pharmaceutical preparations of the present invention may be prepared and formulated as emulsions. Emulsions are usually heterogeneous systems of one liquid dispersed in another in the form of droplets usually exceeding 0.1 m in diameter. The emulsions of the present invention may contain excipients such as emulsifiers, stabilizers, dyes, fats, oils, waxes, fatty acids, fatty alcohols, fatty esters, humectants, hydrophilic colloids, preservatives, and anti-oxidants may also be present in emulsions as needed. These excipients may be present as a solution in either the aqueous phase, oily phase or itself as a separate phase.

Examples of naturally occurring emulsifiers that may be used in emulsion formulations of the present invention include lanolin, beeswax, phosphatides, lecithin and acacia. Finely divided solids have also been used as good emulsifiers especially in combination with surfactants and in viscous preparations. Examples of finely divided solids that may be used as emulsifiers include polar inorganic solids, such as heavy metal hydroxides, nonswelling clays such as bentonite, attapulgite, hectorite, kaolin, montmorillonite, colloidal aluminum silicate and colloidal magnesium aluminum silicate, pigments and nonpolar solids such as carbon or glyceryl tristearate.

Examples of preservatives that may be included in the emulsion formulations include methyl paraben, propyl paraben, quaternary ammonium salts, benzalkonium chloride, esters of p-hydroxybenzoic acid, and boric acid. Examples of antioxidants that may be included in the emulsion formulations include free radical scavengers such as tocopherols, alkyl gallates, butylated hydroxyanisole, butylated hydroxytoluene, or reducing agents such as ascorbic acid and sodium metabisulfite, and antioxidant synergists such as citric acid, tartaric acid, and lecithin.

In one embodiment, the compositions of oligonucleotides are formulated as microemulsions. A microemulsion is a system of water, oil and amphiphile which is a single optically isotropic and thermodynamically stable liquid solution. Typically microemulsions are prepared by first dispersing an oil in an aqueous surfactant solution and then adding a sufficient amount of a 4th component, generally an intermediate chain-length alcohol to form a transparent system.

Surfactants that may be used in the preparation of microemulsions include, but are not limited to, ionic surfactants, non-ionic surfactants, Brij 96, polyoxyethylene oleyl ethers, polyglycerol fatty acid esters, tetraglycerol monolaurate (ML310), tetraglycerol monooleate (MO310), hexaglycerol monooleate (PO310), hexaglycerol pentaoleate (PO500), decaglycerol monocaprate (MCA750), decaglycerol monooleate (MO750), decaglycerol sequioleate (S0750), decaglycerol decaoleate (DA0750), alone or in combination with cosurfactants. The cosurfactant, usually a short-chain alcohol such as ethanol, 1-propanol, and 1-butanol, serves to increase the interfacial fluidity by penetrating into the surfactant film and consequently creating a disordered film because of the void space generated among surfactant molecules.

Microemulsions may, however, be prepared without the use of cosurfactants and alcohol-free self-emulsifying microemulsion systems are known in the art. The aqueous phase may typically be, but is not limited to, water, an aqueous solution of the drug, glycerol, PEG300, PEG400, polyglycerols, propylene glycols, and derivatives of ethylene glycol. The oil phase may include, but is not limited to, materials such as Captex 300, Captex 355, Capmul MCM, fatty acid esters, medium chain (C₈-C₁₂) mono, di, and tri-glycerides, polyoxyethylated glyceryl fatty acid esters, fatty alcohols, polyglycolized glycerides, saturated polyglycolized C₈-C₁₀ glycerides, vegetable oils and silicone oil.

Microemulsions are particularly of interest from the standpoint of drug solubilization and the enhanced absorption of drugs. Lipid based microemulsions (both oil/water and water/oil) have been proposed to enhance the oral bioavailability of drugs.

Microemulsions offer improved drug solubilization, protection of drug from enzymatic hydrolysis, possible enhancement of drug absorption due to surfactant-induced alterations in membrane fluidity and permeability, ease of preparation, ease of oral administration over solid dosage forms, improved clinical potency, and decreased toxicity (Constantinides et al., Pharmaceutical Research, 1994, 11:1385; Ho et al., J. Pharm. Sci., 1996, 85:138-143). Microemulsions have also been effective in the transdermal delivery of active components in both cosmetic and pharmaceutical applications. It is expected that the microemulsion compositions and formulations of the present invention will facilitate the increased systemic absorption of oligonucleotides from the gastrointestinal tract, as well as improve the local cellular uptake of oligonucleotides within the gastrointestinal tract, vagina, buccal cavity and other areas of administration.

In an embodiment, the present invention employs various penetration enhancers to affect the efficient delivery of nucleic acids, particularly oligonucleotides, to the skin of animals. Even non-lipophilic drugs may cross cell membranes if the membrane to be crossed is treated with a penetration enhancer. In addition to increasing the diffusion of non-lipophilic drugs across cell membranes, penetration enhancers also act to enhance the permeability of lipophilic drugs.

Five categories of penetration enhancers that may be used in the present invention include: surfactants, fatty acids, bile salts, chelating agents, and non-chelating non-surfactants. Other agents may be utilized to enhance the penetration of the administered oligonucleotides include: glycols such as ethylene glycol and propylene glycol, pyrrols such as 2-15 pyrrol, azones, and terpenes such as limonene, and menthone.

The oligonucleotides, especially in lipid formulations, can also be administered by coating a medical device, for example, a catheter, such as an angioplasty balloon catheter, with a cationic lipid formulation. Coating may be achieved, for example, by dipping the medical device into a lipid formulation or a mixture of a lipid formulation and a suitable solvent, for example, an aqueous-based buffer, an aqueous solvent, ethanol, methylene chloride, chloroform and the like. An amount of the formulation will naturally adhere to the surface of the device which is subsequently administered to a patient, as appropriate. Alternatively, a lyophilized mixture of a lipid formulation may be specifically bound to the surface of the device. Such binding techniques are described, for example, in K. Ishihara et al., Journal of Biomedical Materials Research, Vol. 27, pp. 1309-1314 (1993), the disclosures of which are incorporated herein by reference in their entirety.

The useful dosage to be administered and the particular mode of administration will vary depending upon such factors as the cell type, or for in vivo use, the age, weight and the particular animal and region thereof to be treated, the particular oligonucleotide and delivery method used, the therapeutic or diagnostic use contemplated, and the form of the formulation, for example, suspension, emulsion, micelle or liposome, as will be readily apparent to those skilled in the art. Typically, dosage is administered at lower levels and increased until the desired effect is achieved. When lipids are used to deliver the oligonucleotides, the amount of lipid compound that is administered can vary and generally depends upon the amount of oligonucleotide agent being administered. For example, the weight ratio of lipid compound to oligonucleotide agent is preferably from about 1:1 to about 15:1, with a weight ratio of about 5:1 to about 10:1 being more preferred. Generally, the amount of cationic lipid compound which is administered will vary from between about 0.1 milligram (mg) to about 1 gram (g). By way of general guidance, typically between about 0.1 mg and about 10 mg of the particular oligonucleotide agent, and about 1 mg to about 100 mg of the lipid compositions, each per kilogram of patient body weight, is administered, although higher and lower amounts can be used.

The agents of the invention are administered to subjects or contacted with cells in a biologically compatible form suitable for pharmaceutical administration. By “biologically compatible form suitable for administration” is meant that the oligonucleotide is administered in a form in which any toxic effects are outweighed by the therapeutic effects of the oligonucleotide. In one embodiment, oligonucleotides can be administered to subjects. Examples of subjects include mammals, e.g., humans and other primates; cows, pigs, horses, and farming (agricultural) animals; dogs, cats, and other domesticated pets; mice, rats, and transgenic non-human animals.

Administration of an active amount of an oligonucleotide of the present invention is defined as an amount effective, at dosages and for periods of time necessary to achieve the desired result. For example, an active amount of an oligonucleotide may vary according to factors such as the type of cell, the oligonucleotide used, and for in vivo uses the disease state, age, sex, and weight of the individual, and the ability of the oligonucleotide to elicit a desired response in the individual. Establishment of therapeutic levels of oligonucleotides within the cell is dependent upon the rates of uptake and efflux or degradation. Decreasing the degree of degradation prolongs the intracellular half-life of the oligonucleotide. Thus, chemically-modified oligonucleotides, e.g., with modification of the phosphate backbone, may require different dosing.

The exact dosage of an oligonucleotide and number of doses administered will depend upon the data generated experimentally and in clinical trials. Several factors such as the desired effect, the delivery vehicle, disease indication, and the route of administration, will affect the dosage. Dosages can be readily determined by one of ordinary skill in the art and formulated into the subject pharmaceutical compositions. Preferably, the duration of treatment will extend at least through the course of the disease symptoms.

Dosage regime may be adjusted to provide the optimum therapeutic response. For example, the oligonucleotide may be repeatedly administered, e.g., several doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation. One of ordinary skill in the art will readily be able to determine appropriate doses and schedules of administration of the subject oligonucleotides, whether the oligonucleotides are to be administered to cells or to subjects.

Physical methods of introducing nucleic acids include injection of a solution containing the nucleic acid, bombardment by particles covered by the nucleic acid, soaking the cell or organism in a solution of the nucleic acid, or electroporation of cell membranes in the presence of the nucleic acid. A viral construct packaged into a viral particle would accomplish both efficient introduction of an expression construct into the cell and transcription of nucleic acid encoded by the expression construct. Other methods known in the art for introducing nucleic acids to cells may be used, such as lipid-mediated carrier transport, chemical-mediated transport, such as calcium phosphate, and the like. Thus the nucleic acid may be introduced along with components that perform one or more of the following activities: enhance nucleic acid uptake by the cell, inhibit annealing of single strands, stabilize the single strands, or other-wise increase inhibition of the target gene.

Nucleic acid may be directly introduced into the cell (i.e., intracellularly); or introduced extracellularly into a cavity, interstitial space, into the circulation of an organism, introduced orally, or may be introduced by bathing a cell or organism in a solution containing the nucleic acid. Vascular or extravascular circulation, the blood or lymph system, and the cerebrospinal fluid are sites where the nucleic acid may be introduced.

The cell with the target gene may be derived from or contained in any organism. The organism may a plant, animal, protozoan, bacterium, virus, or fungus. The plant may be a monocot, dicot or gymnosperm; the animal may be a vertebrate or invertebrate. Preferred microbes are those used in agriculture or by industry, and those that are pathogenic for plants or animals.

Alternatively, vectors, e.g., transgenes encoding a siRNA of the invention can be engineered into a host cell or transgenic animal using art recognized techniques.

A further preferred use for the agents of the present invention (or vectors or transgenes encoding same) is a functional analysis to be carried out in eukaryotic cells, or eukaryotic non-human organisms, preferably mammalian cells or organisms and most preferably human cells, e.g. cell lines such as HeLa or 293 or rodents, e.g. rats and mice. By administering a suitable priming agent/RNAi agent which is sufficiently complementary to a target mRNA sequence to direct target-specific RNA interference, a specific knockout or knockdown phenotype can be obtained in a target cell, e.g. in cell culture or in a target organism.

Thus, a further subject matter of the invention is a eukaryotic cell or a eukaryotic non-human organism exhibiting a target gene-specific knockout or knockdown phenotype comprising a fully or at least partially deficient expression of at least one endogenous target gene wherein said cell or organism is transfected with at least one vector comprising DNA encoding an RNAi agent capable of inhibiting the expression of the target gene. It should be noted that the present invention allows a target-specific knockout or knockdown of several different endogenous genes due to the specificity of the RNAi agent.

Gene-specific knockout or knockdown phenotypes of cells or non-human organisms, particularly of human cells or non-human mammals may be used in analytic to procedures, e.g. in the functional and/or phenotypical analysis of complex physiological processes such as analysis of gene expression profiles and/or proteomes. Preferably the analysis is carried out by high throughput methods using oligonucleotide based chips.

Assays of Oligonucleotide Stability

In some embodiments, the oligonucleotides of the invention are stabilized, i.e., substantially resistant to endonuclease and exonuclease degradation. An oligonucleotide is defined as being substantially resistant to nucleases when it is at least about 3-fold more resistant to attack by an endogenous cellular nuclease, and is highly nuclease resistant when it is at least about 6-fold more resistant than a corresponding oligonucleotide. This can be demonstrated by showing that the oligonucleotides of the invention are substantially resistant to nucleases using techniques which are known in the art.

One way in which substantial stability can be demonstrated is by showing that the oligonucleotides of the invention function when delivered to a cell, e.g., that they reduce transcription or translation of target nucleic acid molecules, e.g., by measuring protein levels or by measuring cleavage of mRNA. Assays which measure the stability of target RNA can be performed at about 24 hours post-transfection (e.g., using Northern blot techniques, RNase Protection Assays, or QC-PCR assays as known in the art). Alternatively, levels of the target protein can be measured. Preferably, in addition to testing the RNA or protein levels of interest, the RNA or protein levels of a control, non-targeted gene will be measured (e.g., actin, or preferably a control with sequence similarity to the target) as a specificity control. RNA or protein measurements can be made using any art-recognized technique. Preferably, measurements will be made beginning at about 16-24 hours post transfection. (M. Y. Chiang, et al. 1991. J Biol Chem. 266:18162-71; T. Fisher, et al. 1993. Nucleic Acids Research. 21 3857).

The ability of an oligonucleotide composition of the invention to inhibit protein synthesis can be measured using techniques which are known in the art, for example, by detecting an inhibition in gene transcription or protein synthesis. For example, Nuclease S mapping can be performed. In another example, Northern blot analysis can be used to measure the presence of RNA encoding a particular protein. For example, total RNA can be prepared over a cesium chloride cushion (see, e.g., Ausebel et al., 1987. Current Protocols in Molecular Biology (Greene & Wiley, New York)). Northern blots can then be made using the RNA and probed (see, e.g., Id.). In another example, the level of the specific mRNA produced by the target protein can be measured, e.g., using PCR. In yet another example, Western blots can be used to measure the amount of target protein present. In still another embodiment, a phenotype influenced by the amount of the protein can be detected. Techniques for performing Western blots are well known in the art, see, e.g., Chen et al. J. Biol. Chem. 271:28259.

In another example, the promoter sequence of a target gene can be linked to a reporter gene and reporter gene transcription (e.g., as described in more detail below) can be monitored. Alternatively, oligonucleotide compositions that do not target a promoter can be identified by fusing a portion of the target nucleic acid molecule with a reporter gene so that the reporter gene is transcribed. By monitoring a change in the expression of the reporter gene in the presence of the oligonucleotide composition, it is possible to determine the effectiveness of the oligonucleotide composition in inhibiting the expression of the reporter gene. For example, in one embodiment, an effective oligonucleotide composition will reduce the expression of the reporter gene.

A “reporter gene” is a nucleic acid that expresses a detectable gene product, which may be RNA or protein. Detection of mRNA expression may be accomplished by Northern blotting and detection of protein may be accomplished by staining with antibodies specific to the protein. Preferred reporter genes produce a readily detectable product. A reporter gene may be operably linked with a regulatory DNA sequence such that detection of the reporter gene product provides a measure of the transcriptional activity of the regulatory sequence. In preferred embodiments, the gene product of the reporter gene is detected by an intrinsic activity associated with that product. For instance, the reporter gene may encode a gene product that, by enzymatic activity, gives rise to a detectable signal based on color, fluorescence, or luminescence. Examples of reporter genes include, but are not limited to, those coding for chloramphenicol acetyl transferase (CAT), luciferase, beta-galactosidase, and alkaline phosphatase.

One skilled in the art would readily recognize numerous reporter genes suitable for use in the present invention. These include, but are not limited to, chloramphenicol acetyltransferase (CAT), luciferase, human growth hormone (hGH), and beta-galactosidase. Examples of such reporter genes can be found in F. A. Ausubel et al., Eds., Current Protocols in Molecular Biology, John Wiley & Sons, New York, (1989). Any gene that encodes a detectable product, e.g., any product having detectable enzymatic activity or against which a specific antibody can be raised, can be used as a reporter gene in the present methods.

One reporter gene system is the firefly luciferase reporter system. (Gould, S. J., and Subramani, S. 1988. Anal. Biochem., 7:404-408 incorporated herein by reference). The luciferase assay is fast and sensitive. In this assay, a lysate of the test cell is prepared and combined with ATP and the substrate luciferin. The encoded enzyme luciferase catalyzes a rapid, ATP dependent oxidation of the substrate to generate a light-emitting product. The total light output is measured and is proportional to the amount of luciferase present over a wide range of enzyme concentrations.

CAT is another frequently used reporter gene system; a major advantage of this system is that it has been an extensively validated and is widely accepted as a measure of promoter activity. (Gorman C. M., Moffat, L. F., and Howard, B. H. 1982. Mol. Cell. Biol., 2:1044-1051). In this system, test cells are transfected with CAT expression vectors and incubated with the candidate substance within 2-3 days of the initial transfection. Thereafter, cell extracts are prepared. The extracts are incubated with acetyl CoA and radioactive chloramphenicol. Following the incubation, acetylated chloramphenicol is separated from nonacetylated form by thin layer chromatography. In this assay, the degree of acetylation reflects the CAT gene activity with the particular promoter.

Another suitable reporter gene system is based on immunologic detection of hGH. This system is also quick and easy to use. (Selden, R., Burke-Howie, K. Rowe, M. E., Goodman, H. M., and Moore, D. D. (1986), Mol. Cell, Biol., 6:3173-3179 incorporated herein by reference). The hGH system is advantageous in that the expressed hGH polypeptide is assayed in the media, rather than in a cell extract. Thus, this system does not require the destruction of the test cells. It will be appreciated that the principle of this reporter gene system is not limited to hGH but rather adapted for use with any polypeptide for which an antibody of acceptable specificity is available or can be prepared.

In one embodiment, nuclease stability of a double-stranded oligonucleotide of the invention is measured and compared to a control, e.g., an RNAi molecule typically used in the art (e.g., a duplex oligonucleotide of less than 25 nucleotides in length and comprising 2 nucleotide base overhangs) or an unmodified RNA duplex with blunt ends.

The target RNA cleavage reaction achieved using the siRNAs of the invention is highly sequence specific. Sequence identity may determined by sequence comparison and alignment algorithms known in the art. To determine the percent identity of two nucleic acid sequences (or of two amino acid sequences), the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in the first sequence or second sequence for optimal alignment). A preferred, non-limiting example of a local alignment algorithm utilized for the comparison of sequences is the algorithm of Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 87:2264-68, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873-77. Such an algorithm is incorporated into the BLAST programs (version 2.0) of Altschul, et al. (1990) J. Mol. Biol. 215:403-10. Greater than 90% sequence identity, e.g., 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or even 100% sequence identity, between the siRNA and the portion of the target gene is preferred. Alternatively, the siRNA may be defined functionally as a nucleotide sequence (or oligonucleotide sequence) that is capable of hybridizing with a portion of the target gene transcript. Examples of stringency conditions for polynucleotide hybridization are provided in Sambrook, J., E. F. Fritsch, and T. Maniatis, 1989, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., chapters 9 and 11, and Current Protocols in Molecular Biology, 1995, F. M. Ausubel et al., eds., John Wiley & Sons, Inc., sections 2.10 and 6.3-6.4, incorporated herein by reference.

Therapeutic Use

By inhibiting the expression of a gene, the oligonucleotide compositions of the present invention can be used to treat any disease involving the expression of a protein. Examples of diseases that can be treated by oligonucleotide compositions, just to illustrate, include: cancer, retinopathies, autoimmune diseases, inflammatory diseases (i.e., ICAM-1 related disorders, Psoriasis, Ulcerative Colitus, Crohn's disease), viral diseases (i.e., HIV, Hepatitis C), miRNA disorders, and cardiovascular diseases.

In one embodiment, in vitro treatment of cells with oligonucleotides can be used for ex vivo therapy of cells removed from a subject (e.g., for treatment of leukemia or viral infection) or for treatment of cells which did not originate in the subject, but are to be administered to the subject (e.g., to eliminate transplantation antigen expression on cells to be transplanted into a subject). In addition, in vitro treatment of cells can be used in non-therapeutic settings, e.g., to evaluate gene function, to study gene regulation and protein synthesis or to evaluate improvements made to oligonucleotides designed to modulate gene expression or protein synthesis. In vivo treatment of cells can be useful in certain clinical settings where it is desirable to inhibit the expression of a protein. There are numerous medical conditions for which antisense therapy is reported to be suitable (see, e.g., U.S. Pat. No. 5,830,653) as well as respiratory syncytial virus infection (WO 95/22,553) influenza virus (WO 94/23,028), and malignancies (WO 94/08,003). Other examples of clinical uses of antisense sequences are reviewed, e.g., in Glaser. 1996. Genetic Engineering News 16:1. Exemplary targets for cleavage by oligonucleotides include, e.g., protein kinase Ca, ICAM-1, c-raf kinase, p53, c-myb, and the bcr/abl fusion gene found in chronic myelogenous leukemia.

The subject nucleic acids can be used in RNAi-based therapy in any animal having RNAi pathway, such as human, non-human primate, non-human mammal, non-human vertebrates, rodents (mice, rats, hamsters, rabbits, etc.), domestic livestock animals, pets (cats, dogs, etc.), Xenopus, fish, insects (Drosophila, etc.), and worms (C. elegans), etc.

The invention provides methods for preventing in a subject, a disease or condition associated with an aberrant or unwanted target gene expression or activity, by administering to the subject a therapeutic agent (e.g., a RNAi agent or vector or transgene encoding same). If appropriate, subjects are first treated with a priming agent so as to be more responsive to the subsequent RNAi therapy. Subjects at risk for a disease which is caused or contributed to by aberrant or unwanted target gene expression or activity can be identified by, for example, any or a combination of diagnostic or prognostic assays as described herein. Administration of a prophylactic agent can occur prior to the manifestation of symptoms characteristic of the target gene aberrancy, such that a disease or disorder is prevented or, alternatively, delayed in its progression. Depending on the type of target gene aberrancy, for example, a target gene, target gene agonist or target gene antagonist agent can be used for treating the subject.

In another aspect, the invention pertains to methods of modulating target gene expression, protein expression or activity for therapeutic purposes. Accordingly, in an exemplary embodiment, the modulatory method of the invention involves contacting a cell capable of expressing target gene with a therapeutic agent of the invention that is specific for the target gene or protein (e.g., is specific for the mRNA encoded by said gene or specifying the amino acid sequence of said protein) such that expression or one or more of the activities of target protein is modulated. These modulatory methods can be performed in vitro (e.g., by culturing the cell with the agent), in vivo (e.g., by administering the agent to a subject), or ex vivo. Typically, subjects are first treated with a priming agent so as to be more responsive to the subsequent RNAi therapy. As such, the present invention provides methods of treating an individual afflicted with a disease or disorder characterized by aberrant or unwanted expression or activity of a target gene polypeptide or nucleic acid molecule. Inhibition of target gene activity is desirable in situations in which target gene is abnormally unregulated and/or in which decreased target gene activity is likely to have a beneficial effect.

The therapeutic agents of the invention can be administered to individuals to treat (prophylactically or therapeutically) disorders associated with aberrant or unwanted target gene activity. In conjunction with such treatment, pharmacogenomics (i.e., the study of the relationship between an individual's genotype and that individual's response to a foreign compound or drug) may be considered. Differences in metabolism of therapeutics can lead to severe toxicity or therapeutic failure by altering the relation between dose and blood concentration of the pharmacologically active drug. Thus, a physician or clinician may consider applying knowledge obtained in relevant pharmacogenomics studies in determining whether to administer a therapeutic agent as well as tailoring the dosage and/or therapeutic regimen of treatment with a therapeutic agent. Pharmacogenomics deals with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, for example, Eichelbaum, M. et al. (1996) Clin. Exp. Pharmacol. Physiol. 23(10-11): 983-985 and Linder, M. W. et al. (1997) Clin. Chem. 43(2):254-266

RNAi in Skin Indications

Nucleic acid molecules, or compositions comprising nucleic acid molecules, described herein may in some embodiments be administered to pre-treat, treat or prevent compromised skin. As used herein “compromised skin” refers to skin which exhibits characteristics distinct from normal skin. Compromised skin may occur in association with a dermatological condition. Several non-limiting examples of dermatological conditions include rosacea, common acne, seborrheic dermatitis, perioral dermatitis, acneform rashes, transient acantholytic dermatosis, and acne necrotica miliaris. In some instances, compromised skin may comprise a wound and/or scar tissue. In some instances, methods and compositions associated with the invention may be used to promote wound healing, prevention, reduction or inhibition of scarring, and/or promotion of re-epithelialisation of wounds.

A subject can be pre-treated or treated prophylactically with a molecule associated with the invention, prior to the skin of the subject becoming compromised. As used herein “pre-treatment” or “prophylactic treatment” refers to administering a nucleic acid to the skin prior to the skin becoming compromised. For example, a subject could be pre-treated 15 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 7 hours, 8 hours, 9 hours, 10 hours, 11 hours, 12 hours, 24 hours, 48 hours, or more than 48 hours prior to the skin becoming compromised. In other embodiments, a subject can be treated with a molecule associated with the invention immediately before the skin becomes compromised and/or simultaneous to the skin becoming compromised and/or after the skin has been compromised. In some embodiments, the skin is compromised through a medical procedure such as surgery, including elective surgery. In certain embodiments methods and compositions may be applied to areas of the skin that are believed to be at risk of becoming compromised. It should be appreciated that one of ordinary skill in the art would be able to optimize timing of administration using no more than routine experimentation.

In some aspects, methods associated with the invention can be applied to promote healing of compromised skin. Administration can occur at any time up until the compromised skin has healed, even if the compromised skin has already partially healed. The timing of administration can depend on several factors including the nature of the compromised skin, the degree of damage within the compromised skin, and the size of the compromised area. In some embodiments administration may occur immediately after the skin is compromised, or 30 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 8 hours, 12 hours, 24 hours, 48 hours, or more than 48 hours after the skin has been compromised. Methods and compositions of the invention may be administered one or more times as necessary. For example, in some embodiments, compositions may be administered daily or twice daily. In some instances, compositions may be administered both before and after formation of compromised skin.

Compositions associated with the invention may be administered by any suitable route. In some embodiments, administration occurs locally at an area of compromised skin. For example, compositions may be administered by intradermal injection. Compositions for intradermal injection may include injectable solutions. Intradermal injection may in some embodiments occur around the are of compromised skin or at a site where the skin is likely to become compromised. In some embodiments, compositions may also be administered in a topical form, such as in a cream or ointment. In some embodiments, administration of compositions described herein comprises part of an initial treatment or pre-treatment of compromised skin, while in other embodiments, administration of such compositions comprises follow-up care for an area of compromised skin.

The appropriate amount of a composition or medicament to be applied can depend on many different factors and can be determined by one of ordinary skill in the art through routine experimentation. Several non-limiting factors that might be considered include biological activity and bioavailability of the agent, nature of the agent, mode of administration, half-life, and characteristics of the subject to be treated.

In some aspects, nucleic acid molecules associated with the invention may also be used in treatment and/or prevention of fibrotic disorders, including pulmonary fibrosis, liver cirrhosis, scleroderma and glomerulonephritis, lung fibrosis, liver fibrosis, skin fibrosis, muscle fibrosis, radiation fibrosis, kidney fibrosis, proliferative vitreoretinopathy and uterine fibrosis.

A therapeutically effective amount of a nucleic acid molecule described herein may in some embodiments be an amount sufficient to prevent the formation of compromised skin and/or improve the condition of compromised skin. In some embodiments, improvement of the condition of compromised skin may correspond to promotion of wound healing and/or inhibition of scarring and/or promotion of epithelial regeneration. The extent of prevention of formation of compromised skin and/or improvement to the condition of compromised skin may in some instances be determined by, for example, a doctor or clinician.

The ability of nucleic acid molecules associated with the invention to prevent the formation of compromised skin and/or improve the condition of compromised skin may in some instances be measured with reference to properties exhibited by the skin. In some instances, these properties may include rate of epithelialisation and/or decreased size of an area of compromised skin compared to control skin at comparable time points.

As used herein, prevention of formation of compromised skin, for example prior to a surgical procedure, and/or improvement of the condition of compromised skin, for example after a surgical procedure, can encompass any increase in the rate of healing in the compromised skin as compared with the rate of healing occurring in a control sample. In some instances, the condition of compromised skin may be assessed with respect to either comparison of the rate of re-epithelialisation achieved in treated and control skin, or comparison of the relative areas of treated and control areas of compromised skin at comparable time points. In some aspects, a molecule that prevents formation of compromised skin or promotes healing of compromised skin may be a molecule that, upon administration, causes the area of compromised skin to exhibit an increased rate of re-epithelialisation and/or a reduction of the size of compromised skin compared to a control at comparable time points. In some embodiments, the healing of compromised skin may give rise to a rate of healing that is 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or 100% greater than the rate occurring in controls.

In some aspects, subjects to be treated by methods and compositions associated with the invention may be subjects who will undergo, are undergoing or have undergone a medical procedure such as a surgery. In some embodiments, the subject may be prone to defective, delayed or otherwise impaired re-epithelialisation, such as dermal wounds in the aged. Other non-limiting examples of conditions or disorders in which wound healing is associated with delayed or otherwise impaired re-epithelialisation include patients suffering from diabetes, patients with polypharmacy, post-menopausal women, patients susceptible to pressure injuries, patients with venous disease, clinically obese patients, patients receiving chemotherapy, patients receiving radiotherapy, patients receiving steroid treatment, and immuno-compromised patients. In some instances, defective re-epithelialisation response can contributes to infections at the wound site, and to the formation of chronic wounds such as ulcers.

In some embodiments, methods associated with the invention may promote the re-epithelialisation of compromised skin in chronic wounds, such as ulcers, and may also inhibit scarring associated with wound healing. In other embodiments, methods associated with the invention are applied to prevention or treatment of compromised skin in acute wounds in patients predisposed to impaired wound healing developing into chronic wounds. In other aspects, methods associated with the invention are applied to promote accelerated healing of compromised skin while preventing, reducing or inhibiting scarring for use in general clinical contexts. In some aspects, this can involve the treatment of surgical incisions and application of such methods may result in the prevention, reduction or inhibition of scarring that may otherwise occur on such healing. Such treatment may result in the scars being less noticeable and exhibiting regeneration of a more normal skin structure. In other embodiments, the compromised skin that is treated is not compromised skin that is caused by a surgical incision. The compromised skin may be subject to continued care and continued application of medicaments to encourage re-epithelialisation and healing.

In some aspects, methods associated with the invention may also be used in the treatment of compromised skin associated with grafting procedures. This can involve treatment at a graft donor site and/or at a graft recipient site. Grafts can in some embodiments involve skin, artificial skin, or skin substitutes. Methods associated with the invention can also be used for promoting epithelial regeneration. As used herein, promotion of epithelial regeneration encompasses any increase in the rate of epithelial regeneration as compared to the regeneration occurring in a control-treated or untreated epithelium. The rate of epithelial regeneration attained can in some instances be compared with that taking place in control-treated or untreated epithelia using any suitable model of epithelial regeneration known in the art. Promotion of epithelial regeneration may be of use to induce effective re-epithelialisation in contexts in which the re-epithelialisation response is impaired, inhibited, retarded or otherwise defective. Promotion of epithelial regeneration may be also effected to accelerate the rate of defective or normal epithelial regeneration responses in patients suffering from epithelial damage.

Some instances where re-epithelialisation response may be defective include conditions such as pemphigus, Hailey-Hailey disease (familial benign pemphigus), toxic epidermal necrolysis (TEN)/Lyell's syndrome, epidermolysis bullosa, cutaneous leishmaniasis and actinic keratosis. Defective re-epithelialisation of the lungs may be associated with idiopathic pulmonary fibrosis (IPF) or interstitial lung disease. Defective re-epithelialisation of the eye may be associated with conditions such as partial limbal stem cell deficiency or corneal erosions. Defective re-epithelialisation of the gastrointestinal tract or colon may be associated with conditions such as chronic anal fissures (fissure in ano), ulcerative colitis or Crohn's disease, and other inflammatory bowel disorders.

In some aspects, methods associated with the invention are used to prevent, reduce or otherwise inhibit compromised skin associated with scarring. This can be applied to any site within the body and any tissue or organ, including the skin, eye, nerves, tendons, ligaments, muscle, and oral cavity (including the lips and palate), as well as internal organs (such as the liver, heart, brain, abdominal cavity, pelvic cavity, thoracic cavity, guts and reproductive tissue). In the skin, treatment may change the morphology and organization of collagen fibers and may result in making the scars less visible and blend in with the surrounding skin. As used herein, prevention, reduction or inhibition of scarring encompasses any degree of prevention, reduction or inhibition in scarring as compared to the level of scarring occurring in a control-treated or untreated wound.

Prevention, reduction or inhibition of compromised skin, such as compromised skin associated with dermal scarring, can be assessed and/or measured with reference to microscopic and/or macroscopic characteristics. Macroscopic characteristics may include color, height, surface texture and stiffness of the skin. In some instances, prevention, reduction or inhibition of compromised skin may be demonstrated when the color, height, surface texture and stiffness of the skin resembles that of normal skin more closely after treatment than does a control that is untreated. Microscopic assessment of compromised skin may involve examining characteristics such as thickness and/or orientation and/or composition of the extracellular matrix (ECM) fibers, and cellularity of the compromised skin. In some instances, prevention, reduction or inhibition of compromised skin may be demonstrated when the thickness and/or orientation and/or composition of the extracellular matrix (ECM) fibers, and/or cellularity of the compromised skin resembles that of normal skin more closely after treatment than does a control that is untreated.

In some aspects, methods associated with the invention are used for cosmetic purposes, at least in part to contribute to improving the cosmetic appearance of compromised skin. In some embodiments, methods associated with the invention may be used to prevent, reduce or inhibit compromised skin such as scarring of wounds covering joints of the body. In other embodiments, methods associated with the invention may be used to promote accelerated wound healing and/or prevent, reduce or inhibit scarring of wounds at increased risk of forming a contractile scar, and/or of wounds located at sites of high skin tension.

In some embodiments, methods associated with the invention can be applied to promoting healing of compromised skin in instances where there is an increased risk of pathological scar formation, such as hypertrophic scars and keloids, which may have more pronounced deleterious effects than normal scarring. In some embodiments, methods described herein for promoting accelerated healing of compromised skin and/or preventing, reducing or inhibiting scarring are applied to compromised skin produced by surgical revision of pathological scars.

Aspects of the invention can be applied to compromised skin caused by burn injuries. Healing in response to burn injuries can lead to adverse scarring, including the formation of hypertrophic scars. Methods associated with the invention can be applied to treatment of all injuries involving damage to an epithelial layer, such as injuries to the skin in which the epidermis is damaged. Other non-limiting examples of injuries to epithelial tissue include injuries involving the respiratory epithelia, digestive epithelia or epithelia surrounding internal tissues or organs.

Target Genes

It should be appreciated that based on the RNAi molecules designed and disclosed herein, one of ordinary skill in the art would be able to design such RNAi molecules to target a variety of different genes depending on the context and intended use. For purposes of pre-treating, treating, or preventing compromised skin and/or promoting wound healing and/or preventing, reducing or inhibiting scarring, one of ordinary skill in the art would appreciate that a variety of suitable target genes could be identified based at least in part on the known or predicted functions of the genes, and/or the known or predicted expression patterns of the genes. Several non-limiting examples of genes that could be targeted by RNAi molecules for pre-treating, treating, or preventing compromised skin and/or promoting wound healing and/or preventing, reducing or inhibiting scarring include genes that encode for the following proteins: Transforming growth factor β (TGFβ1, TGFβ2, TGFβ3), Osteopontin, Connective tissue growth factor (CTGF), Platelet-derived growth factor (PDGF), Hypoxia inducible factor-1α (HIF1α), Collagen I and/or III, Prolyl 4-hydroxylase (P4H), Procollagen C-protease (PCP), Matrix metalloproteinase 2, 9 (MMP2, 9), Integrins, Connexin, Histamine H1 receptor, Tissue transglutaminase, Mammalian target of rapamycin (mTOR), HoxB13, VEGF, IL-6, SMAD proteins, Ribosomal protein S6 kinases (RSP6) and Cyclooxygenase-2 (COX-2).

Transforming growth factor β proteins, for which three isoforms exist in mammals (TGFβ1, TGFβ2, TGFβ3), are secreted proteins belonging to a superfamily of growth factors involved in the regulation of many cellular processes including proliferation, migration, apoptosis, adhesion, differentiation, inflammation, immuno-suppression and expression of extracellular proteins. These proteins are produced by a wide range of cell types including epithelial, endothelial, hematopoietic, neuronal, and connective tissue cells. Representative Genbank accession numbers providing DNA and protein sequence information for human TGFβ1, TGFβ2 and TGFβ3 are BT007245, BC096235, and X14149, respectively. Within the TGFβ family, TGFβ1 and TGFβ2 but not TGFβ3 represent suitable targets. The alteration in the ratio of TGFβ variants will promote better wound healing and will prevent excessive scar formation. Osteopontin (OPN), also known as Secreted phosphoprotein 1 (SPP1), Bone Sinaloprotein 1 (BSP-1), and early T-lymphocyte activation (ETA-1) is a secreted glycoprotein protein that binds to hydroxyapatite. OPN has been implicated in a variety of biological processes including bone remodeling, immune functions, chemotaxis, cell activation and apoptosis. Osteopontin is produced by a variety of cell types including fibroblasts, preosteoblasts, osteoblasts, osteocytes, odontoblasts, bone marrow cells, hypertrophic chondrocytes, dendritic cells, macrophages, smooth muscle, skeletal muscle myoblasts, endothelial cells, and extraosseous (non-bone) cells in the inner ear, brain, kidney, deciduum, and placenta. Representative Genbank accession number providing DNA and protein sequence information for human Osteopontin are NM_000582.2 and X13694.

Connective tissue growth factor (CTGF), also known as Hypertrophic chondrocyte-specific protein 24, is a secreted heparin-binding protein that has been implicated in wound healing and scleroderma. Connective tissue growth factor is active in many cell types including fibroblasts, myofibroblasts, endothelial and epithelial cells. Representative Genbank accession number providing DNA and protein sequence information for human CTGF are NM_001901.2 and M92934.

The Platelet-derived growth factor (PDGF) family of proteins, including several isoforms, are secreted mitogens. PDGF proteins are implicated in wound healing, at least in part, because they are released from platelets following wounding. Representative Genbank accession numbers providing DNA and protein sequence information for human PDGF genes and proteins include X03795 (PDGFA), X02811 (PDGFB), AF091434 (PDGFC), AB033832 (PDGFD).

Hypoxia inducible factor-1α (HIF1α), is a transcription factor involved in cellular response to hypoxia. HIF1α is implicated in cellular processes such as embryonic vascularization, tumor angiogenesis and pathophysiology of ischemic disease. A representative Genbank accession number providing DNA and protein sequence information for human HIF1α is U22431.

Collagen proteins are the most abundant mammalian proteins and are found in tissues such as skin, tendon, vascular, ligature, organs, and bone. Collagen I proteins (such as COL1A1 and COL1A2) are detected in scar tissue during wound healing, and are expressed in the skin. Collagen III proteins (including COL3A1) are detected in connective tissue in wounds (granulation tissue), and are also expressed in skin. Representative Genbank accession numbers providing DNA and protein sequence information for human Collagen proteins include: Z74615 (COL1A1), J03464 (COL1A2) and X14420 (COL3A1).

Prolyl 4-hydroxylase (P4H), is involved in production of collagen and in oxygen sensing. A representative Genbank accession number providing DNA and protein sequence information for human P4H is AY198406.

Procollagen C-protease (PCP) is another target.

Matrix metalloproteinase 2, 9 (MMP2, 9) belong to the metzincin metalloproteinase superfamily and are zinc-dependent endopeptidases. These proteins are implicated in a variety of cellular processes including tissue repair. Representative Genbank accession numbers providing DNA and protein sequence information for human MMP proteins are M55593 (MMP2) and J05070 (MMP9).

Integrins are a family of proteins involved in interaction and communication between a cell and the extracellular matrix. Vertebrates contain a variety of integrins including α₁β₁, α₂β₁, α₄β₁, α₅β₁, α₆β₁, α_(L)β₂, α_(M)β₂, α_(11b)β₃, α_(v)β₃, α_(v)β₅, α_(v)β₆, α₆β₄.

Connexins are a family of vertebrate transmembrane proteins that form gap junctions. Several examples of Connexins, with the accompanying gene name shown in brackets, include Cx23 (GJE1), Cx25 (GJB7), Cx26 (GJB2), Cx29 (GJE1), Cx30 (GJB6), Cx30.2 (GJC3), Cx30.3 (GJB4), Cx31 (GJB3), Cx31.1 (GJB5), Cx31.9 (GJC1/GJD3), Cx32 (GJB1), Cx33 (GJA6), Cx36 (GJD2/GJA9), Cx37 (GJA4), Cx39 (GJD4), Cx40 (GJA5), Cx40.1 (GJD4), Cx43 (GJA1), Cx45 (GJC1/GJA7), Cx46 (GJA3), Cx47 (GJC2/GJA12), Cx50 (GJA8), Cx59 (GJA10), and Cx62 (GJA10).

Histamine H1 receptor (HRH1) is a metabotropic G-protein-coupled receptor involved in the phospholipase C and phosphatidylinositol (PIP2) signaling pathways. A representative Genbank accession number providing DNA and protein sequence information for human HRH1 is Z34897.

Tissue transglutaminase, also called Protein-glutamine gamma-glutamyltransferase 2, is involved in protein crosslinking and is implicated is biological processes such as apoptosis, cellular differentiation and matrix stabilization. A representative Genbank accession number providing DNA and protein sequence information for human Tissue transglutaminase is M55153.

Mammalian target of rapamycin (mTOR), also known as Serine/threonine-protein kinase mTOR and FK506 binding protein 12-rapamycin associated protein 1 (FRAP1), is involved in regulating cell growth and survival, cell motility, transcription and translation. A representative Genbank accession number providing DNA and protein sequence information for human mTOR is L34075.

HoxB13 belongs to the family of Homeobox proteins and has been linked to functions such as cutaneous regeneration and fetal skin development. A representative Genbank accession number providing DNA and protein sequence information for human HoxB13 is U57052.

Vascular endothelial growth factor (VEGF) proteins are growth factors that bind to tyrosine kinase receptors and are implicated in multiple disorders such as cancer, age-related macular degeneration, rheumatoid arthritis and diabetic retinopathy. Members of this protein family include VEGF-A, VEGF-B, VEGF-C and VEGF-D. Representative Genbank accession numbers providing DNA and protein sequence information for human VEGF proteins are M32977 (VEGF-A), U43368 (VEGF-B), X94216 (VEGF-C), and D89630 (VEGF-D).

Interleukin-6 (IL-6) is a cytokine involved in stimulating immune response to tissue damage. A representative Genbank accession number providing DNA and protein sequence information for human IL-6 is X04430.

SMAD proteins (SMAD1-7, 9) are a family of transcription factors involved in regulation of TGFβ signaling. Representative Genbank accession numbers providing DNA and protein sequence information for human SMAD proteins are U59912 (SMAD1), U59911 (SMAD2), U68019 (SMAD3), U44378 (SMAD4), U59913 (SMAD5), U59914 (SMAD6), AF015261 (SMAD7), and BC011559 (SMAD9).

Ribosomal protein S6 kinases (RSK6) represent a family of serine/threonine kinases involved in activation of the transcription factor CREB. A representative Genbank accession number providing DNA and protein sequence information for human Ribosomal protein S6 kinase alpha-6 is AF184965.

Cyclooxygenase-2 (COX-2), also called Prostaglandin G/H synthase 2 (PTGS2), is involved in lipid metabolism and biosynthesis of prostanoids and is implicated in inflammatory disorders such as rheumatoid arthritis. A representative Genbank accession number providing DNA and protein sequence information for human COX-2 is AY462100.

EXAMPLES Example 1: Inhibition of Gene Expression Using Minimum Length Trigger RNAs

Transfection of Minimum Length Trigger (mlt) RNA

mltRNA constructs were chemically synthesized (Integrated DNA Technologies, Coralville, Iowa) and transfected into HEK293 cells (ATCC, Manassas, Va.) using the Lipofectamine RNAiMAX (Invitrogen, Carlsbad, Calif.) reagent according to manufacturer's instructions. In brief, RNA was diluted to a 12× concentration and then combined with a 12× concentration of Lipofectamine RNAiMAX to complex. The RNA and transfection reagent were allowed to complex at room temperature for 20 minutes and make a 6× concentration. While complexing, HEK293 cells were washed, trypsinized and counted. The cells were diluted to a concentration recommended by the manufacturer and previously described conditions which was at 1×10⁵ cells/mi. When RNA had completed complexing with the RNAiMAX transfection reagent, 20ul of the complexes were added to the appropriate well of the 96-well plate in triplicate. Cells were added to each well (100ul volume) to make the final cell count per well at 1×10⁴ cells/well. The volume of cells diluted the 6× concentration of complex to IX which was equal to a concentration noted (between 10-0.05 nM). Cells were incubated for 24 or 48 hours under normal growth conditions.

After 24 or 48 hour incubation cells were lysed and gene silencing activity was measured using the QuantiGene assay (Panomics, Freemont, Calif.) which employs bDNA hybridization technology. The assay was carried out according to manufacturer's instructions.

ΔG Calculation

ΔG was calculated using Mfold, available through the Mfold internet site (http://mfold.bioinfo.rpi.edu/cgi-bin/rna-form1.cgi). Methods for calculating ΔG are described in, and are incorporated by reference from, the following references: Zuker, M. (2003) Nucleic Acids Res., 31(13):3406-15; Mathews, D. H., Sabina, J., Zuker, M. and Turner, D. H. (1999) J. Mol. Biol. 288:911-940; Mathews, D. H., Disney, M. D., Childs, J. L., Schroeder, S. J., Zuker, M., and Turner, D. H. (2004) Proc. Natl. Acad. Sci. 101:7287-7292; Duan, S., Mathews, D. H., and Turner, D. H. (2006) Biochemistry 45:9819-9832; Wuchty, S., Fontana, W., Hofacker, I. L., and Schuster, P. (1999) Biopolymers 49:145-165.

Example 2: Optimization of Sd-rxRNA^(nano) Molecules for Gene Silencing

Asymmetric double stranded RNAi molecules, with minimal double stranded regions, were developed herein and are highly effective at gene silencing. These molecules can contain a variety of chemical modifications on the sense and/or anti-sense strands, and can be conjugated to sterol-like compounds such as cholesterol.

FIGS. 1-3 present schematics of RNAi molecules associated with the invention. In the asymmetric molecules, which contain a sense and anti-sense strand, either of the strands can be the longer strand. Either strand can also contain a single-stranded region. There can also be mismatches between the sense and anti-sense strand, as indicated in FIG. 1D. Preferably, one end of the double-stranded molecule is either blunt-ended or contains a short overhang such as an overhang of one nucleotide. FIG. 2 indicates types of chemical modifications applied to the sense and anti-sense strands including 2′F, 2′OMe, hydrophobic modifications and phosphorothioate modifications. Preferably, the single stranded region of the molecule contains multiple phosphorothioate modifications. Hydrophobicity of molecules can be increased using such compounds as 4-pyridyl at 5-U, 2-pyridyl at 5-U, isobutyl at 5-U and indolyl at 5-U (FIG. 2). Proteins or peptides such as protamine (or other Arg rich peptides), spermidine or other similar chemical structures can also be used to block duplex charge and facilitate cellular entry (FIG. 3). Increased hydrophobicity can be achieved through either covalent or non-covalent modifications. Several positively charged chemicals, which might be used for polynucleotide charge blockage are depicted in FIG. 4.

Chemical modifications of polynucleotides, such as the guide strand in a duplex molecule, can facilitate RISC entry. FIG. 5 depicts single stranded polynucleotides, representing a guide strand in a duplex molecule, with a variety of chemical modifications including 2′d, 2′OMe, 2′F, hydrophobic modifications, phosphorothioate modifications, and attachment of conjugates such as “X” in FIG. 5, where X can be a small molecule with high affinity to a PAZ domain, or sterol-type entity. Similarly, FIG. 6 depicts single stranded polynucleotides, representing a passenger strand in a duplex molecule, with proposed structural and chemical compositions of RISC substrate inhibitors. Combinations of chemical modifications can ensure efficient uptake and efficient binding to preloaded RISC complexes.

FIG. 7 depicts structures of polynucleotides with sterol-type molecules attached, where R represents a polycarbonic tail of 9 carbons or longer. FIG. 8 presents examples of naturally occurring phytosterols with a polycarbon chain longer than 8 attached at position 17. More than 250 different types of phytosterols are known. FIG. 9 presents examples of sterol-like structures with variations in the sizes of the polycarbon chains attached at position 17. FIG. 91 presents further examples of sterol-type molecules that can be used as a hydrophobic entity in place of cholesterol. FIG. 92 presents further examples of hydrophobic molecules that might be used as hydrophobic entities in place of cholesterol. Optimization of such characteristics can improve uptake properties of the RNAi molecules. FIG. 10 presents data adapted from Martins et al. (J Lipid Research), showing that the percentage of liver uptake and plasma clearance of lipid emulsions containing sterol-type molecules is directly affected by the size of the attached polycarbon chain at position 17. FIG. 11 depicts a micelle formed from a mixture of polynucleotides attached to hydrophobic conjugates and fatty acids. FIG. 12 describes how alteration in lipid composition can affect pharmacokinetic behavior and tissue distribution of hydrophobically modified and/or hydrophobically conjugated polynucleotides. In particular, the use of lipid mixtures that are enriched in linoleic acid and cardiolipin results in preferential uptake by cardiomyocites.

FIG. 13 depicts examples of RNAi constructs and controls designed to target MAP4K4 expression. FIGS. 14 and 15 reveal that RNAi constructs with minimal duplex regions (such as duplex regions of approximately 13 nucleotides) are effective in mediating RNA silencing in cell culture. Parameters associated with these RNA molecules are shown in FIG. 16. FIG. 17 depicts examples of RNAi constructs and controls designed to target SOD1 expression. FIGS. 18 and 19 reveal the results of gene silencing experiments using these RNAi molecules to target SOD1 in cells. FIG. 20 presents a schematic indicating that RNA molecules with double stranded regions that are less than 10 nucleotides are not cleaved by Dicer, and FIG. 21 presents a schematic of a hypothetical RNAi model for RNA induced gene silencing.

The RNA molecules described herein were subject to a variety of chemical modifications on the sense and antisense strands, and the effects of such modifications were observed. RNAi molecules were synthesized and optimized through testing of a variety of modifications. In first generation optimization, the sense (passenger) and anti-sense (guide) strands of the sd-rxRNA^(nano) molecules were modified for example through incorporation of C and U 2′OMe modifications, 2′F modifications, phosphorothioate modifications, phosphorylation, and conjugation of cholesterol. Molecules were tested for inhibition of MAP4K4 expression in cells including HeLa, primary mouse hepatocytes and primary human hepatocytes through both lipid-mediated and passive uptake transfection.

FIG. 22 reveals that chemical modifications can enhance gene silencing. In particular, modifying the guide strand with 2′F UC modifications, and with a stretch of phosphorothioate modifications, combined with complete CU O′Me modification of the passenger strands, resulted in molecules that were highly effective in gene silencing. The effect of chemical modification on in vitro efficacy in un-assisted delivery in HeLa cells was also examined. FIG. 23 reveals that compounds lacking any of 2′F, 2′OMe, a stretch of phosphorothioate modifications, or cholesterol conjugates, were completely inactive in passive uptake. A combination of all 4 types of chemical modifications, for example in compound 12386, was found to be highly effective in gene silencing. FIG. 24 also shows the effectiveness of compound 12386 in gene silencing.

Optimization of the length of the oligonucleotide was also investigated. FIGS. 25 and 26 reveal that oligonucleotides with a length of 21 nucleotides were more effective than oligonucleotides with a length of 25 nucleotides, indicating that reduction in the size of an RNA molecule can improve efficiency, potentially by assisting in its uptake. Screening was also conducted to optimize the size of the duplex region of double stranded RNA molecules. FIG. 88 reveals that compounds with duplexes of 10 nucleotides were effective in inducing gene silencing. Positioning of the sense strand relative to the guide strand can also be critical for silencing gene expression (FIG. 89). In this assay, a blunt end was found to be most effective. 3′ overhangs were tolerated, but 5′ overhangs resulted in a complete loss of functionality. The guide strand can be effective in gene silencing when hybridized to a sense strand of varying lengths (FIG. 90). In this assay presented in FIG. 90, the compounds were introduced into HeLa cells via lipid mediated transfection.

The importance of phosphorothioate content of the RNA molecule for unassisted delivery was also investigated. FIG. 27 presents the results of a systematic screen that identified that the presence of at least 2-12 phosphorothioates in the guide strand as being highly advantageous for achieving uptake, with 4-8 being the preferred number. FIG. 27 also shows that presence or absence of phosphorothioate modifications in the sense strand did not alter efficacy.

FIGS. 28-29 reveal the effects of passive uptake of RNA compounds on gene silencing in primary mouse hepatocytes. nanoRNA molecules were found to be highly effective, especially at a concentration of 1 μM (FIG. 28). FIGS. 30 and 31 reveal that the RNA compounds associated with the invention were also effective in gene silencing following passive uptake in primary human hepatocytes. The cellular localization of the RNA molecules associated with the invention was examined and compared to the localization of Chol-siRNA (Alnylam) molecules, as shown in FIGS. 32 and 33.

A summary of 1^(st) generation sd-rxRNA molecules is presented in FIG. 21. Chemical modifications were introduced into the RNA molecules, at least in part, to increase potency, such as through optimization of nucleotide length and phosphorothioate content, to reduce toxicity, such as through replacing 2′F modifications on the guide strand with other modifications, to improve delivery such as by adding or conjugating the RNA molecules to linker and sterol modalities, and to improve the ease of manufacturing the RNA molecules. FIG. 35 presents schematic depictions of some of the chemical modifications that were screened in 1^(st) generation molecules. Parameters that were optimized for the guide strand included nucleotide length (e.g., 19, 21 and 25 nucleotides), phosphorothioate content (e.g., 0-18 phosphorothioate linkages) and replacement of 2′F groups with 2′OMe and 5 Me C or riboThymidine. Parameters that were optimized for the sense strand included nucleotide length (e.g., 11, 13 and 19 nucleotides), phosphorothioate content (e.g., 0-4 phosphorothioate linkages), and 2′OMe modifications. FIG. 36 summarizes parameters that were screened. For example, the nucleotide length and the phosphorothioate tail length were modified and screened for optimization, as were the additions of 2′OMe C and U modifications. Guide strand length and the length of the phosphorothioate modified stretch of nucleotides were found to influence efficacy (FIGS. 37-38). Phosphorothioate modifications were tolerated in the guide strand and were found to influence passive uptake (FIGS. 39-42).

FIG. 43 presents a schematic revealing guide strand chemical modifications that were screened. FIGS. 44 and 45 reveal that 2′OMe modifications were tolerated in the 3′ end of the guide strand. In particular, 2′OMe modifications in positions 1 and 11-18 were well tolerated. The 2′OMe modifications in the seed area were tolerated but resulted in slight reduction of efficacy. Ribo-modifications in the seed were also well tolerated. These data indicate that the molecules associated with the invention offer the significant advantage of having reduced or no 2′F modification content. This is advantageous because 2′F modifications are thought to generate toxicity in vivo. In some instances, a complete substitution of 2′F modifications with 2′OMe was found to lead to some reduction in potency. However, the 2′ OMe substituted molecules were still very active. A molecule with 50% reduction in 2′F content (including at positions 11, 16-18 which were changed to 2′OMe modifications), was found to have comparable efficacy to a compound with complete 2′F C and U modification. 2′OMe modification in position was found in some instances to reduce efficacy, although this can be at least partially compensated by 2′OMe modification in position 1 (with chemical phosphate). In some instances, 5 Me C and/or ribothymidine substitution for 2′F modifications led to a reduction in passive uptake efficacy, but increased potency in lipid mediated transfections compared to 2′F modifications. Optimization results for lipid mediated transfection were not necessarily the same as for passive uptake.

Modifications to the sense strand were also developed and tested, as depicted in FIG. 46. FIG. 47 reveals that in some instances, a sense strand length between 10-15 bases was found to be optimal. For the molecules tested in FIG. 47, an increase in the sense strand length resulted in reduction of passive uptake, however an increase in sense strand length may be tolerated for some compounds. FIG. 47 also reveals that LNA modification of the sense strand demonstrated similar efficacy to non-LNA containing compounds. In general, the addition of LNA or other thermodynamically stabilizing compounds has been found to be beneficial, in some instances resulting in converting non-functional sequences to functional sequences. FIG. 48 also presents data on sense strand length optimization, while FIG. 49 shows that phosphorothioate modification of the sense strand is not required for passive uptake.

Based on the above-described optimization experiments, 2^(nd) generation RNA molecules were developed. As shown in FIG. 50, these molecules contained reduced phosphorothioate modification content and reduced 2′F modification content, relative to 1^(st) generation RNA molecules. Significantly, these RNA molecules exhibit spontaneous cellular uptake and efficacy without a delivery vehicle (FIG. 51). These molecules can achieve self-delivery (i.e., with no transfection reagent) and following self-delivery can exhibit nanomolar activity in cell culture. These molecules can also be delivered using lipid-mediated transfection, and exhibit picomolar activity levels following transfection. Significantly, these molecules exhibit highly efficient uptake, 95% by most cells in cell culture, and are stable for more than three days in the presence of 100% human serum. These molecules are also highly specific and exhibit little or no immune induction. FIGS. 52 and 53 reveal the significance of chemical modifications and the configurations of such modifications in influencing the properties of the RNA molecules associated with the invention.

Linker chemistry was also tested in conjunction with the RNA molecules associated with the invention. As depicted in FIG. 54, 2^(nd) generation RNA molecules were synthesized with sterol-type molecules attached through TEG and amino caproic acid linkers. Both linkers showed identical potency. This functionality of the RNA molecules, independent of linker chemistry offers additional advantages in terms of scale up and synthesis and demonstrates that the mechanism of function of these RNA molecules is very different from other previously described RNA molecules.

Stability of the chemically modified sd-rxRNA molecules described herein in human serum is shown in FIG. 55 in comparison to unmodified RNA. The duplex molecules were incubated in 75% serum at 37° C. for the indicated periods of time. The level of degradation was determined by running the samples on non-denaturing gels and staining with SYBGR.

FIGS. 56 and 57 present data on cellular uptake of the sd-rxRNA molecules. FIG. 56 shows that minimizing the length of the RNA molecule is importance for cellular uptake, while FIG. 57 presents data showing target gene silencing after spontaneous cellular uptake in mouse PEC-derived macrophages. FIG. 58 demonstrates spontaneous uptake and target gene silencing in primary cells. FIG. 59 shows the results of delivery of sd-rxRNA molecules associated with the invention to RPE cells with no formulation. Imaging with Hoechst and DY547 reveals the clear presence of a signal representing the RNA molecule in the sd-rxRNA sample, while no signal is detectable in the other samples including the samples competing a competing conjugate, an rxRNA, and an untransfected control. FIG. 60 reveals silencing of target gene expression in RPE cells treated with sd-rxRNA molecules associated with the invention following 24-48 hours without any transfection formulation.

FIG. 61 shows further optimization of the chemical/structural composition of sd-rxRNA compounds. In some instances, preferred properties included an antisense strand that was 17-21 nucleotides long, a sense strand that was 10-15 nucleotides long, phosphorothioate modification of 2-12 nucleotides within the single stranded region of the molecule, preferentially phosphorothioate modification of 6-8 nucleotides within the single stranded region, and 2′OMe modification at the majority of positions within the sense strand, with or without phosphorothioate modification. Any linker chemistry can be used to attach the hydrophobic moiety, such as cholesterol, to the 3′ end of the sense strand. Version GIIb molecules, as shown in FIG. 61, have no 2′F modifications. Significantly, there is was no impact on efficacy in these molecules.

FIG. 62 demonstrates the superior performance of sd-rxRNA compounds compared to compounds published by Wolfrum et. al. Nature Biotech, 2007. Both generation I and II compounds (GI and GIIa) developed herein show great efficacy in reducing target gene expression. By contrast, when the chemistry described in Wolfrum et al. (all oligos contain cholesterol conjugated to the 3′ end of the sense strand) was applied to the same sequence in a context of conventional siRNA (19 bp duplex with two overhang) the compound was practically inactive. These data emphasize the significance of the combination of chemical modifications and assymetrical molecules described herein, producing highly effective RNA compounds.

FIG. 63 shows localization of sd-rxRNA molecules developed herein compared to localization of other RNA molecules such as those described in Soutschek et al. (2004) Nature, 432:173. sd-rxRNA molecules accumulate inside the cells whereas competing conjugate RNAs accumulate on the surface of cells. Significantly, FIG. 64 shows that sd-rxRNA molecules, but not competitor molecules such as those described in Soutschek et al. are internalized within minutes. FIG. 65 compares localization of sd-rxRNA molecules compared to regular siRNA-cholesterol, as described in Soutschek et al. A signal representing the RNA molecule is clearly detected for the sd-rxRNA molecule in tissue culture RPE cells, following local delivery to compromised skin, and following systemic delivery where uptake to the liver is seen. In each case, no signal is detected for the regular siRNA-cholesterol molecule. The sd-rxRNA molecule thus has drastically better cellular and tissue uptake characteristics when compared to conventional cholesterol conjugated siRNAs such as those described in Soutschek et al. The level of uptake is at least order of magnitude higher and is due at least in part to the unique combination of chemistries and conjugated structure. Superior delivery of sd-rxRNA relative to previously described RNA molecules is also demonstrated in FIGS. 66 and 67.

Based on the analysis of 2^(nd) generation RNA molecules associated with the invention, a screen was performed to identify functional molecules for targeting the SPP1/PPIB gene. As revealed in FIG. 68, several effective molecules were identified, with 14131 being the most effective. The compounds were added to A-549 cells and then the level of SPP1/PPIB ratio was determined by B-DNA after 48 hours.

FIG. 69 reveals efficient cellular uptake of sd-rxRNA within minutes of exposure. This is a unique characteristics of these molecules, not observed with any other RNAi compounds. Compounds described in Soutschek et al. were used as negative controls. FIG. 70 reveals that the uptake and gene silencing of the sd-rxRNA is effective in multiple different cell types including SH-SY5Y neuroblastoma derived cells, ARPE-19 (retinal pigment epithelium) cells, primary hepatocytes, and primary macrophages. In each case silencing was confirmed by looking at target gene expression by a Branched DNA assay.

FIG. 70 reveals that sd-rxRNA is active in the presence or absence of serum. While a slight reduction in efficacy (2-5 fold) was observed in the presence of serum, this small reduction in efficacy in the presence of serum differentiate the sd-rxRNA molecules from previously described molecules which exhibited a larger reduction in efficacy in the presence of serum. This demonstrated level of efficacy in the presence of serum creates a foundation for in vivo efficacy.

FIG. 72 reveals efficient tissue penetration and cellular uptake upon single intradermal injection. This data indicates the potential of the sd-rxRNA compounds described herein for silencing genes in any dermatology applications, and also represents a model for local delivery of sd-rxRNA compounds. FIG. 73 also demonstrates efficient cellular uptake and in vivo silencing with sd-rxRNA following intradermal injection. Silencing is determined as the level of MAP4K4 knockdown in several individual biopsies taken from the site of injection as compared to biopsies taken from a site injected with a negative control. FIG. 74 reveals that sd-rxRNA compounds has improved blood clearance and induced effective gene silencing in vivo in the liver upon systemic administration. In comparison to the RNA molecules described by Soutschek et al., the level of liver uptake at identical dose level is at least 50 fold higher with the sd-rxRNA molecules. The uptake results in productive silencing. sd-rxRNA compounds are also characterized by improved blood clearance kinetics.

The effect of 5-Methly C modifications was also examined. FIG. 75 demonstrates that the presence of 5-Methyl C in an RNAi molecule resulted in increased potency in lipid mediated transfection. This suggests that hydrophobic modification of Cs and Us in an RNAi molecule can be beneficial. These types of modifications can also be used in the context 2′ ribose modified bases to ensure optimal stability and efficacy. FIG. 76 presents data showing that incorporation of 5-Methyl C and/or ribothymidine in the guide strand can in some instances reduce efficacy.

FIG. 77 reveals that sd-rxRNA molecules are more effective than competitor molecules such as molecules described in Soutschek et al., in systemic delivery to the liver. A signal representing the RNA molecule is clearly visible in the sample containing sd-rxRNA, while no signal representing the RNA molecule is visible in the sample containing the competitor RNA molecule.

The addition of hydrophobic conjugates to the sd-rxRNA molecules was also explored (FIGS. 78-83). FIG. 78 presents schematics demonstrating 5-uridyl modifications with improved hydrophobicity characteristics. Incorporation of such modifications into sd-rxRNA compounds can increase cellular and tissue uptake properties. FIG. 78B presents a new type of RNAi compound modification which can be applied to compounds to improve cellular uptake and pharmacokinetic behavior. Significantly, this type of modification, when applied to sd-rxRNA compounds, may contribute to making such compounds orally available. FIG. 79 presents schematics revealing the structures of synthesized modified sterol-type molecules, where the length and structure of the C17 attached tail is modified. Without wishing to be bound by any theory, the length of the C17 attached tail may contribute to improving in vitro and in vivo efficacy of sd-rxRNA compounds.

FIG. 80 presents a schematic demonstrating the lithocholic acid route to long side chain cholesterols. FIG. 81 presents a schematic demonstrating a route to 5-uridyl phosphoramidite synthesis. FIG. 82 presents a schematic demonstrating synthesis of tri-functional hydroxyprolinol linker for 3′-cholesterol attachment. FIG. 83 presents a schematic demonstrating synthesis of solid support for the manufacture of a shorter asymmetric RNAi compound strand.

A screen was conducted to identify compounds that could effectively silence expression of SPP1 (Osteopontin). Compounds targeting SPP1 were added to A549 cells (using passive transfection), and the level of SPP1 expression was evaluated at 48 hours. Several novel compounds effective in SPP1 silencing were identified. Compounds that were effective in silencing of SPP1 included 14116, 14121, 14131, 14134, 14139, 14149, and 14152 (FIGS. 84-86). The most potent compound in this assay was 14131 (FIG. 84). The efficacy of these sd-rxRNA compounds in silencing SPP1 expression was independently validated (FIG. 85).

A similar screen was conducted to identify compounds that could effectively silence expression of CTGF (FIGS. 86-87). Compounds that were effective in silencing of CTGF included 14017, 14013, 14016, 14022, 14025, 14027.

Methods Transfection of Sd-rxRNA^(nano) Lipid Mediated Transfection

sd-rxRNA^(nano) constructs were chemically synthesized (Dharmacon, Lafayette, Colo.) and transfected into HEK293 cells (ATCC, Manassas, Va.) using Lipofectamine RNAiMAX (Invitrogen, Carlsbad, Calif.) according to the manufacturer's instructions. In brief, RNA was diluted to a 12× concentration in Opti-MEM®1 Reduced Serum Media (Invitrogen, Carlsbad, Calif.) and then combined with a 12× concentration of Lipofectamine RNAiMAX. The RNA and transfection reagent were allowed to complex at room temperature for 20 minutes and make a 6× concentration. While complexing, HEK293 cells were washed, trypsinized and counted. The cells were diluted to a concentration recommended by the manufacturer and previously described of 1×10⁵cells/ml. When RNA had completed complexing with the RNAiMAX transfection reagent, 20 ul of the complexes were added to the appropriate well of the 96-well plate in triplicate. Cells were added to each well (100 ul volume) to make the final cell count per well 1×10⁴ cells/well. The volume of cells diluted the 6× concentration of complex to 1× (between 10-0.05 nM). Cells were incubated for 24 or 48 hours under normal growth conditions. After 24 or 48 hour incubation, cells were lysed and gene silencing activity was measured using the QuantiGene assay (Panomics, Freemont, Calif.) which employs bDNA hybridization technology. The assay was carried out according to manufacturer's instructions.

Passive Uptake Transfection

sd-rxRNA^(nano) constructs were chemically synthesized (Dharmacon, Lafayette, Colo.). 24 hours prior to transfection, HeLa cells (ATCC, Manassas, Va.) were plated at 1×10⁴ cells/well in a 96 well plate under normal growth conditions (DMEM, 10% FBS and 1% Penicillin and Streptomycin). Prior to transfection of HeLa cells, sd-rxRNA^(nano) were diluted to a final concentration of 0.01 uM to 1 uM in Accell siRNA Delivery Media (Dharmacon, Lafayette, Colo.). Normal growth media was aspirated off cells and 100 uL of Accell Delivery media containing the appropriate concentration of sd-rxRNAnano was applied to the cells. 48 hours post transfection, delivery media was aspirated off the cells and normal growth media was applied to cells for an additional 24 hours.

After 48 or 72 hour incubation, cells were lysed and gene silencing activity was measured using the QuantiGene assay (Panomics, Freemont, Calif.) according to manufacturer's instructions.

TABLE 1 Oligo Accession Gene ID Number Number number Gene Name Symbol APOB-10167- 12138 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 20-12138 APOB-10167- 12139 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 20-12139 MAP4K4-2931- 12266 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 13-12266 (MAP4K4), transcript variant 1 MAP4K4-2931- 12293 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12293 (MAP4K4), transcript variant 1 MAP4K4-2931- 12383 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12383 (MAP4K4), transcript variant 1 MAP4K4-2931- 12384 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12384 (MAP4K4), transcript variant 1 MAP4K4-2931- 12385 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12385 (MAP4K4), transcript variant 1 MAP4K4-2931- 12386 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12386 (MAP4K4), transcript variant 1 MAP4K4-2931- 12387 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12387 (MAP4K4), transcript variant 1 MAP4K4-2931- 12388 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 15-12388 (MAP4K4), transcript variant 1 MAP4K4-2931- 12432 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 13-12432 (MAP4K4), transcript variant 1 MAP4K4-2931- 12266.2 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 13-12266.2 (MAP4K4), transcript variant 1 APOB--21- 12434 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 12434 APOB--21- 12435 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 12435 MAP4K4-2931- 12451 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12451 (MAP4K4), transcript variant 1 MAP4K4-2931- 12452 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12452 (MAP4K4), transcript variant 1 MAP4K4-2931- 12453 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12453 (MAP4K4), transcript variant 1 MAP4K4-2931- 12454 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 17-12454 (MAP4K4), transcript variant 1 MAP4K4-2931- 12455 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 17-12455 (MAP4K4), transcript variant 1 MAP4K4-2931- 12456 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 19-12456 (MAP4K4), transcript variant 1 --27-12480 12480 --27-12481 12481 APOB-10167- 12505 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 21-12505 APOB-10167- 12506 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 21-12506 MAP4K4-2931- 12539 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12539 (MAP4K4), transcript variant 1 APOB-10167- 12505.2 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 21-12505.2 APOB-10167- 12506.2 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 21-12506.2 MAP4K4--13- 12565 MAP4K4 12565 MAP4K4-2931- 12386.2 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 16-12386.2 (MAP4K4), transcript variant 1 MAP4K4-2931- 12815 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 13-12815 (MAP4K4), transcript variant 1 APOB--13- 12957 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 12957 MAP4K4--16- 12983 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12983 (MAP4K4), transcript variant 1 MAP4K4--16- 12984 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12984 (MAP4K4), transcript variant 1 MAP4K4--16- 12985 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12985 (MAP4K4), transcript variant 1 MAP4K4--16- 12986 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12986 (MAP4K4), transcript variant 1 MAP4K4--16- 12987 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12987 (MAP4K4), transcript variant 1 MAP4K4--16- 12988 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12988 (MAP4K4), transcript variant 1 MAP4K4--16- 12989 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12989 (MAP4K4), transcript variant 1 MAP4K4--16- 12990 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12990 (MAP4K4), transcript variant 1 MAP4K4--16- 12991 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12991 (MAP4K4), transcript variant 1 MAP4K4--16- 12992 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12992 (MAP4K4), transcript variant 1 MAP4K4--16- 12993 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12993 (MAP4K4), transcript variant 1 MAP4K4--16- 12994 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12994 (MAP4K4), transcript variant 1 MAP4K4--16- 12995 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 12995 (MAP4K4), transcript variant 1 MAP4K4-2931- 13012 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 19-13012 (MAP4K4), transcript variant 1 MAP4K4-2931- 13016 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 19-13016 (MAP4K4), transcript variant 1 PPIB--13- 13021 NM_000942 Peptidylprolyl Isomerase B (cyclophilin B) PPIB 13021 pGL3-1172- 13038 U47296 Cloning vector pGL3-Control pGL3 13-13038 pGL3-1172- 13040 U47296 Cloning vector pGL3-Control pGL3 13-13040 --16-13047 13047 SOD1-530-13- 13090 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13090 sclerosis 1 (adult)) SOD1-523-13- 13091 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13091 sclerosis 1 (adult)) SOD1-535-13- 13092 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13092 sclerosis 1 (adult)) SOD1-536-13- 13093 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13093 sclerosis 1 (adult)) SOD1-396-13- 13094 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13094 sclerosis 1 (adult)) SOD1-385-13- 13095 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13095 sclerosis 1 (adult)) SOD1-195-13- 13096 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13096 sclerosis 1 (adult)) APOB-4314- 13115 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13-13115 APOB-3384- 13116 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13-13116 APOB-3547- 13117 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13-13117 APOB-4318- 13118 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13-13118 APOB-3741- 13119 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13-13119 PPIB--16- 13136 NM_000942 Peptidylprolyl Isomerase B (cyclophilin B) PPIB 13136 APOB-4314- 13154 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 15-13154 APOB-3547- 13155 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 15-13155 APOB-4318- 13157 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 15-13157 APOB-3741- 13158 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 15-13158 APOB--13- 13159 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13159 APOB--15- 13160 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13160 SOD1-530-16- 13163 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13163 sclerosis 1 (adult)) SOD1-523-16- 13164 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13164 sclerosis 1 (adult)) SOD1-535-16- 13165 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13165 sclerosis 1 (adult)) SOD1-536-16- 13166 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13166 sclerosis 1 (adult)) SOD1-396-16- 13167 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13167 sclerosis 1 (adult)) SOD1-385-16- 13168 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13168 sclerosis 1 (adult)) SOD1-195-16- 13169 NM_000454 Superoxide Dismutase 1, soluble (amyotrophic lateral SOD1 13169 sclerosis 1 (adult)) pGL3-1172- 13170 U47296 Cloning vector pGL3-Control pGL3 16-13170 pGL3-1172- 13171 U47296 Cloning vector pGL3-Control pGL3 16-13171 MAP4k4-2931- 13189 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4k4 19-13189 (MAP4K4), transcript variant 1 CTGF-1222- 13190 NM_001901.2 connective tissue growth factor CTGF 13-13190 CTGF-813-13- 13192 NM_001901.2 connective tissue growth factor CTGF 13192 CTGF-747-13- 13194 NM_001901.2 connective tissue growth factor CTGF 13194 CTGF-817-13- 13196 NM_001901.2 connective tissue growth factor CTGF 13196 CTGF-1174- 13198 NM_001901.2 connective tissue growth factor CTGF 13-13198 CTGF-1005- 13200 NM_001901.2 connective tissue growth factor CTGF 13-13200 CTGF-814-13- 13202 NM_001901.2 connective tissue growth factor CTGF 13202 CTGF-816-13- 13204 NM_001901.2 connective tissue growth factor CTGF 13204 CTGF-1001- 13206 NM_001901.2 connective tissue growth factor CTGF 13-13206 CTGF-1173- 13208 NM_001901.2 connective tissue growth factor CTGF 13-13208 CTGF-749-13- 13210 NM_001901.2 connective tissue growth factor CTGF 13210 CTGF-792-13- 13212 NM_001901.2 connective tissue growth factor CTGF 13212 CTGF-1162- 13214 NM_001901.2 connective tissue growth factor CTGF 13-13214 CTGF-811-13- 13216 NM_001901.2 connective tissue growth factor CTGF 13216 CTGF-797-13- 13218 NM_001901.2 connective tissue growth factor CTGF 13218 CTGF-1175- 13220 NM_001901.2 connective tissue growth factor CTGF 13-13220 CTGF-1172- 13222 NM_001901.2 connective tissue growth factor CTGF 13-13222 CTGF-1177- 13224 NM_001901.2 connective tissue growth factor CTGF 13-13224 CTGF-1176- 13226 NM_001901.2 connective tissue growth factor CTGF 13-13226 CTGF-812-13- 13228 NM_001901.2 connective tissue growth factor CTGF 13228 CTGF-745-13- 13230 NM_001901.2 connective tissue growth factor CTGF 13230 CTGF-1230- 13232 NM_001901.2 connective tissue growth factor CTGF 13-13232 CTGF-920-13- 13234 NM_001901.2 connective tissue growth factor CTGF 13234 CTGF-679-13- 13236 NM_001901.2 connective tissue growth factor CTGF 13236 CTGF-992-13- 13238 NM_001901.2 connective tissue growth factor CTGF 13238 CTGF-1045- 13240 NM_001901.2 connective tissue growth factor CTGF 13-13240 CTGF-1231- 13242 NM_001901.2 connective tissue growth factor CTGF 13-13242 CTGF-991-13- 13244 NM_001901.2 connective tissue growth factor CTGF 13244 CTGF-998-13- 13246 NM_001901.2 connective tissue growth factor CTGF 13246 CTGF-1049- 13248 NM_001901.2 connective tissue growth factor CTGF 13-13248 CTGF-1044- 13250 NM_001901.2 connective tissue growth factor CTGF 13-13250 CTGF-1327- 13252 NM_001901.2 connective tissue growth factor CTGF 13-13252 CTGF-1196- 13254 NM_001901.2 connective tissue growth factor CTGF 13-13254 CTGF-562-13- 13256 NM_001901.2 connective tissue growth factor CTGF 13256 CTGF-752-13- 13258 NM_001901.2 connective tissue growth factor CTGF 13258 CTGF-994-13- 13260 NM_001901.2 connective tissue growth factor CTGF 13260 CTGF-1040- 13262 NM_001901.2 connective tissue growth factor CTGF 13-13262 CTGF-1984- 13264 NM_001901.2 connective tissue growth factor CTGF 13-13264 CTGF-2195- 13266 NM_001901.2 connective tissue growth factor CTGF 13-13266 CTGF-2043- 13268 NM_001901.2 connective tissue growth factor CTGF 13-13268 CTGF-1892- 13270 NM_001901.2 connective tissue growth factor CTGF 13-13270 CTGF-1567- 13272 NM_001901.2 connective tissue growth factor CTGF 13-13272 CTGF-1780- 13274 NM_001901.2 connective tissue growth factor CTGF 13-13274 CTGF-2162- 13276 NM_001901.2 connective tissue growth factor CTGF 13-13276 CTGF-1034- 13278 NM_001901.2 connective tissue growth factor CTGF 13-13278 CTGF-2264- 13280 NM_001901.2 connective tissue growth factor CTGF 13-13280 CTGF-1032- 13282 NM_001901.2 connective tissue growth factor CTGF 13-13282 CTGF-1535- 13284 NM_001901.2 connective tissue growth factor CTGF 13-13284 CTGF-1694- 13286 NM_001901.2 connective tissue growth factor CTGF 13-13286 CTGF-1588- 13288 NM_001901.2 connective tissue growth factor CTGF 13-13288 CTGF-928-13- 13290 NM_001901.2 connective tissue growth factor CTGF 13290 CTGF-1133- 13292 NM_001901.2 connective tissue growth factor CTGF 13-13292 CTGF-912-13- 13294 NM_001901.2 connective tissue growth factor CTGF 13294 CTGF-753-13- 13296 NM_001901.2 connective tissue growth factor CTGF 13296 CTGF-918-13- 13298 NM_001901.2 connective tissue growth factor CTGF 13298 CTGF-744-13- 13300 NM_001901.2 connective tissue growth factor CTGF 13300 CTGF-466-13- 13302 NM_001901.2 connective tissue growth factor CTGF 13302 CTGF-917-13- 13304 NM_001901.2 connective tissue growth factor CTGF 13304 CTGF-1038- 13306 NM_001901.2 connective tissue growth factor CTGF 13-13306 CTGF-1048- 13308 NM_001901.2 connective tissue growth factor CTGF 13-13308 CTGF-1235- 13310 NM_001901.2 connective tissue growth factor CTGF 13-13310 CTGF-868-13- 13312 NM_001901.2 connective tissue growth factor CTGF 13312 CTGF-1131- 13314 NM_001901.2 connective tissue growth factor CTGF 13-13314 CTGF-1043- 13316 NM_001901.2 connective tissue growth factor CTGF 13-13316 CTGF-751-13- 13318 NM_001901.2 connective tissue growth factor CTGF 13318 CTGF-1227- 13320 NM_001901.2 connective tissue growth factor CTGF 13-13320 CTGF-867-13- 13322 NM_001901.2 connective tissue growth factor CTGF 13322 CTGF-1128- 13324 NM_001901.2 connective tissue growth factor CTGF 13-13324 CTGF-756-13- 13326 NM_001901.2 connective tissue growth factor CTGF 13326 CTGF-1234- 13328 NM_001901.2 connective tissue growth factor CTGF 13-13328 CTGF-916-13- 13330 NM_001901.2 connective tissue growth factor CTGF 13330 CTGF-925-13- 13332 NM_001901.2 connective tissue growth factor CTGF 13332 CTGF-1225- 13334 NM_001901.2 connective tissue growth factor CTGF 13-13334 CTGF-445-13- 13336 NM_001901.2 connective tissue growth factor CTGF 13336 CTGF-446-13- 13338 NM_001901.2 connective tissue growth factor CTGF 13338 CTGF-913-13- 13340 NM_001901.2 connective tissue growth factor CTGF 13340 CTGF-997-13- 13342 NM_001901.2 connective tissue growth factor CTGF 13342 CTGF-277-13- 13344 NM_001901.2 connective tissue growth factor CTGF 13344 CTGF-1052- 13346 NM_001901.2 connective tissue growth factor CTGF 13-13346 CTGF-887-13- 13348 NM_001901.2 connective tissue growth factor CTGF 13348 CTGF-914-13- 13350 NM_001901.2 connective tissue growth factor CTGF 13350 CTGF-1039- 13352 NM_001901.2 connective tissue growth factor CTGF 13-13352 CTGF-754-13- 13354 NM_001901.2 connective tissue growth factor CTGF 13354 CTGF-1130- 13356 NM_001901.2 connective tissue growth factor CTGF 13-13356 CTGF-919-13- 13358 NM_001901.2 connective tissue growth factor CTGF 13358 CTGF-922-13- 13360 NM_001901.2 connective tissue growth factor CTGF 13360 CTGF-746-13- 13362 NM_001901.2 connective tissue growth factor CTGF 13362 CTGF-993-13- 13364 NM_001901.2 connective tissue growth factor CTGF 13364 CTGF-825-13- 13366 NM_001901.2 connective tissue growth factor CTGF 13366 CTGF-926-13- 13368 NM_001901.2 connective tissue growth factor CTGF 13368 CTGF-923-13- 13370 NM_001901.2 connective tissue growth factor CTGF 13370 CTGF-866-13- 13372 NM_001901.2 connective tissue growth factor CTGF 13372 CTGF-563-13- 13374 NM_001901.2 connective tissue growth factor CTGF 13374 CTGF-823-13- 13376 NM_001901.2 connective tissue growth factor CTGF 13376 CTGF-1233- 13378 NM_001901.2 connective tissue growth factor CTGF 13-13378 CTGF-924-13- 13380 NM_001901.2 connective tissue growth factor CTGF 13380 CTGF-921-13- 13382 NM_001901.2 connective tissue growth factor CTGF 13382 CTGF-443-13- 13384 NM_001901.2 connective tissue growth factor CTGF 13384 CTGF-1041- 13386 NM_001901.2 connective tissue growth factor CTGF 13-13386 CTGF-1042- 13388 NM_001901.2 connective tissue growth factor CTGF 13-13388 CTGF-755-13- 13390 NM_001901.2 connective tissue growth factor CTGF 13390 CTGF-467-13- 13392 NM_001901.2 connective tissue growth factor CTGF 13392 CTGF-995-13- 13394 NM_001901.2 connective tissue growth factor CTGF 13394 CTGF-927-13- 13396 NM_001901.2 connective tissue growth factor CTGF 13396 SPP1-1025- 13398 NM_000582.2 Osteopontin SPP1 13-13398 SPP1-1049- 13400 NM_000582.2 Osteopontin SPP1 13-13400 SPP1-1051- 13402 NM_000582.2 Osteopontin SPP1 13-13402 SPP1-1048- 13404 NM_000582.2 Osteopontin SPP1 13-13404 SPP1-1050- 13406 NM_000582.2 Osteopontin SPP1 13-13406 SPP1-1047- 13408 NM_000582.2 Osteopontin SPP1 13-13408 SPP1-800-13- 13410 NM_000582.2 Osteopontin SPP1 13410 SPP1-492-13- 13412 NM_000582.2 Osteopontin SPP1 13412 SPP1-612-13- 13414 NM_000582.2 Osteopontin SPP1 13414 SPP1-481-13- 13416 NM_000582.2 Osteopontin SPP1 13416 SPP1-614-13- 13418 NM_000582.2 Osteopontin SPP1 13418 SPP1-951-13- 13420 NM_000582.2 Osteopontin SPP1 13420 SPP1-482-13- 13422 NM_000582.2 Osteopontin SPP1 13422 SPP1-856-13- 13424 NM_000582.2 Osteopontin SPP1 13424 SPP1-857-13- 13426 NM_000582.2 Osteopontin SPP1 13426 SPP1-365-13- 13428 NM_000582.2 Osteopontin SPP1 13428 SPP1-359-13- 13430 NM_000582.2 Osteopontin SPP1 13430 SPP1-357-13- 13432 NM_000582.2 Osteopontin SPP1 13432 SPP1-858-13- 13434 NM_000582.2 Osteopontin SPP1 13434 SPP1-1012- 13436 NM_000582.2 Osteopontin SPP1 13-13436 SPP1-1014- 13438 NM_000582.2 Osteopontin SPP1 13-13438 SPP1-356-13- 13440 NM_000582.2 Osteopontin SPP1 13440 SPP1-368-13- 13442 NM_000582.2 Osteopontin SPP1 13442 SPP1-1011- 13444 NM_000582.2 Osteopontin SPP1 13-13444 SPP1-754-13- 13446 NM_000582.2 Osteopontin SPP1 13446 SPP1-1021- 13448 NM_000582.2 Osteopontin SPP1 13-13448 SPP1-1330- 13450 NM_000582.2 Osteopontin SPP1 13-13450 SPP1-346-13- 13452 NM_000582.2 Osteopontin SPP1 13452 SPP1-869-13- 13454 NM_000582.2 Osteopontin SPP1 13454 SPP1-701-13- 13456 NM_000582.2 Osteopontin SPP1 13456 SPP1-896-13- 13458 NM_000582.2 Osteopontin SPP1 13458 SPP1-1035- 13460 NM_000582.2 Osteopontin SPP1 13-13460 SPP1-1170- 13462 NM_000582.2 Osteopontin SPP1 13-13462 SPP1-1282- 13464 NM_000582.2 Osteopontin SPP1 13-13464 SPP1-1537- 13466 NM_000582.2 Osteopontin SPP1 13-13466 SPP1-692-13- 13468 NM_000582.2 Osteopontin SPP1 13468 SPP1-840-13- 13470 NM_000582.2 Osteopontin SPP1 13470 SPP1-1163- 13472 NM_000582.2 Osteopontin SPP1 13-13472 SPP1-789-13- 13474 NM_000582.2 Osteopontin SPP1 13474 SPP1-841-13- 13476 NM_000582.2 Osteopontin SPP1 13476 SPP1-852-13- 13478 NM_000582.2 Osteopontin SPP1 13478 SPP1-209-13- 13480 NM_000582.2 Osteopontin SPP1 13480 SPP1-1276- 13482 NM_000582.2 Osteopontin SPP1 13-13482 SPP1-137-13- 13484 NM_000582.2 Osteopontin SPP1 13484 SPP1-711-13- 13486 NM_000582.2 Osteopontin SPP1 13486 SPP1-582-13- 13488 NM_000582.2 Osteopontin SPP1 13488 SPP1-839-13- 13490 NM_000582.2 Osteopontin SPP1 13490 SPP1-1091- 13492 NM_000582.2 Osteopontin SPP1 13-13492 SPP1-884-13- 13494 NM_000582.2 Osteopontin SPP1 13494 SPP1-903-13- 13496 NM_000582.2 Osteopontin SPP1 13496 SPP1-1090- 13498 NM_000582.2 Osteopontin SPP1 13-13498 SPP1-474-13- 13500 NM_000582.2 Osteopontin SPP1 13500 SPP1-575-13- 13502 NM_000582.2 Osteopontin SPP1 13502 SPP1-671-13- 13504 NM_000582.2 Osteopontin SPP1 13504 SPP1-924-13- 13506 NM_000582.2 Osteopontin SPP1 13506 SPP1-1185- 13508 NM_000582.2 Osteopontin SPP1 13-13508 SPP1-1221- 13510 NM_000582.2 Osteopontin SPP1 13-13510 SPP1-347-13- 13512 NM_000582.2 Osteopontin SPP1 13512 SPP1-634-13- 13514 NM_000582.2 Osteopontin SPP1 13514 SPP1-877-13- 13516 NM_000582.2 Osteopontin SPP1 13516 SPP1-1033- 13518 NM_000582.2 Osteopontin SPP1 13-13518 SPP1-714-13- 13520 NM_000582.2 Osteopontin SPP1 13520 SPP1-791-13- 13522 NM_000582.2 Osteopontin SPP1 13522 SPP1-813-13- 13524 NM_000582.2 Osteopontin SPP1 13524 SPP1-939-13- 13526 NM_000582.2 Osteopontin SPP1 13526 SPP1-1161- 13528 NM_000582.2 Osteopontin SPP1 13-13528 SPP1-1164- 13530 NM_000582.2 Osteopontin SPP1 13-13530 SPP1-1190- 13532 NM_000582.2 Osteopontin SPP1 13-13532 SPP1-1333- 13534 NM_000582.2 Osteopontin SPP1 13-13534 SPP1-537-13- 13536 NM_000582.2 Osteopontin SPP1 13536 SPP1-684-13- 13538 NM_000582.2 Osteopontin SPP1 13538 SPP1-707-13- 13540 NM_000582.2 Osteopontin SPP1 13540 SPP1-799-13- 13542 NM_000582.2 Osteopontin SPP1 13542 SPP1-853-13- 13544 NM_000582.2 Osteopontin SPP1 13544 SPP1-888-13- 13546 NM_000582.2 Osteopontin SPP1 13546 SPP1-1194- 13548 NM_000582.2 Osteopontin SPP1 13-13548 SPP1-1279- 13550 NM_000582.2 Osteopontin SPP1 13-13550 SPP1-1300- 13552 NM_000582.2 Osteopontin SPP1 13-13552 SPP1-1510- 13554 NM_000582.2 Osteopontin SPP1 13-13554 SPP1-1543- 13556 NM_000582.2 Osteopontin SPP1 13-13556 SPP1-434-13- 13558 NM_000582.2 Osteopontin SPP1 13558 SPP1-600-13- 13560 NM_000582.2 Osteopontin SPP1 13560 SPP1-863-13- 13562 NM_000582.2 Osteopontin SPP1 13562 SPP1-902-13- 13564 NM_000582.2 Osteopontin SPP1 13564 SPP1-921-13- 13566 NM_000582.2 Osteopontin SPP1 13566 SPP1-154-13- 13568 NM_000582.2 Osteopontin SPP1 13568 SPP1-217-13- 13570 NM_000582.2 Osteopontin SPP1 13570 SPP1-816-13- 13572 NM_000582.2 Osteopontin SPP1 13572 SPP1-882-13- 13574 NM_000582.2 Osteopontin SPP1 13574 SPP1-932-13- 13576 NM_000582.2 Osteopontin SPP1 13576 SPP1-1509- 13578 NM_000582.2 Osteopontin SPP1 13-13578 SPP1-157-13- 13580 NM_000582.2 Osteopontin SPP1 13580 SPP1-350-13- 13582 NM_000582.2 Osteopontin SPP1 13582 SPP1-511-13- 13584 NM_000582.2 Osteopontin SPP1 13584 SPP1-605-13- 13586 NM_000582.2 Osteopontin SPP1 13586 SPP1-811-13- 13588 NM_000582.2 Osteopontin SPP1 13588 SPP1-892-13- 13590 NM_000582.2 Osteopontin SPP1 13590 SPP1-922-13- 13592 NM_000582.2 Osteopontin SPP1 13592 SPP1-1169- 13594 NM_000582.2 Osteopontin SPP1 13-13594 SPP1-1182- 13596 NM_000582.2 Osteopontin SPP1 13-13596 SPP1-1539- 13598 NM_000582.2 Osteopontin SPP1 13-13598 SPP1-1541- 13600 NM_000582.2 Osteopontin SPP1 13-13600 SPP1-427-13- 13602 NM_000582.2 Osteopontin SPP1 13602 SPP1-533-13- 13604 NM_000582.2 Osteopontin SPP1 13604 APOB--13- 13763 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13763 APOB--13- 13764 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13764 MAP4K4--16- 13766 MAP4K4 13766 PPIB--13- 13767 NM_000942 peptidylprolyl isomerase B (cyclophilin B) PPIB 13767 PPIB--15- 13768 NM_000942 peptidylprolyl isomerase B (cyclophilin B) PPIB 13768 PPIB--17- 13769 NM_000942 peptidylprolyl isomerase B (cyclophilin B) PPIB 13769 MAP4K4--16- 13939 MAP4K4 13939 APOB-4314- 13940 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 16-13940 APOB-4314- 13941 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 17-13941 APOB--16- 13942 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13942 APOB--18- 13943 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13943 APOB--17- 13944 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13944 APOB--19- 13945 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13945 APOB-4314- 13946 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 16-13946 APOB-4314- 13947 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 17-13947 APOB--16- 13948 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13948 APOB--17- 13949 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13949 APOB--16- 13950 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13950 APOB--18- 13951 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13951 APOB--17- 13952 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13952 APOB--19- 13953 NM_000384 Apolipoprotein B (including Ag(x) antigen) APOB 13953 MAP4K4--16- 13766.2 MAP4K4 13766.2 CTGF-1222- 13980 NM_001901.2 connective tissue growth factor CTGF 16-13980 CTGF-813-16- 13981 NM_001901.2 connective tissue growth factor CTGF 13981 CTGF-747-16- 13982 NM_001901.2 connective tissue growth factor CTGF 13982 CTGF-817-16- 13983 NM_001901.2 connective tissue growth factor CTGF 13983 CTGF-1174- 13984 NM_001901.2 connective tissue growth factor CTGF 16-13984 CTGF-1005- 13985 NM_001901.2 connective tissue growth factor CTGF 16-13985 CTGF-814-16- 13986 NM_001901.2 connective tissue growth factor CTGF 13986 CTGF-816-16- 13987 NM_001901.2 connective tissue growth factor CTGF 13987 CTGF-1001- 13988 NM_001901.2 connective tissue growth factor CTGF 16-13988 CTGF-1173- 13989 NM_001901.2 connective tissue growth factor CTGF 16-13989 CTGF-749-16- 13990 NM_001901.2 connective tissue growth factor CTGF 13990 CTGF-792-16- 13991 NM_001901.2 connective tissue growth factor CTGF 13991 CTGF-1162- 13992 NM_001901.2 connective tissue growth factor CTGF 16-13992 CTGF-811-16- 13993 NM_001901.2 connective tissue growth factor CTGF 13993 CTGF-797-16- 13994 NM_001901.2 connective tissue growth factor CTGF 13994 CTGF-1175- 13995 NM_001901.2 connective tissue growth factor CTGF 16-13995 CTGF-1172- 13996 NM_001901.2 connective tissue growth factor CTGF 16-13996 CTGF-1177- 13997 NM_001901.2 connective tissue growth factor CTGF 16-13997 CTGF-1176- 13998 NM_001901.2 connective tissue growth factor CTGF 16-13998 CTGF-812-16- 13999 NM_001901.2 connective tissue growth factor CTGF 13999 CTGF-745-16- 14000 NM_001901.2 connective tissue growth factor CTGF 14000 CTGF-1230- 14001 NM_001901.2 connective tissue growth factor CTGF 16-14001 CTGF-920-16- 14002 NM_001901.2 connective tissue growth factor CTGF 14002 CTGF-679-16- 14003 NM_001901.2 connective tissue growth factor CTGF 14003 CTGF-992-16- 14004 NM_001901.2 connective tissue growth factor CTGF 14004 CTGF-1045- 14005 NM_001901.2 connective tissue growth factor CTGF 16-14005 CTGF-1231- 14006 NM_001901.2 connective tissue growth factor CTGF 16-14006 CTGF-991-16- 14007 NM_001901.2 connective tissue growth factor CTGF 14007 CTGF-998-16- 14008 NM_001901.2 connective tissue growth factor CTGF 14008 CTGF-1049- 14009 NM_001901.2 connective tissue growth factor CTGF 16-14009 CTGF-1044- 14010 NM_001901.2 connective tissue growth factor CTGF 16-14010 CTGF-1327- 14011 NM_001901.2 connective tissue growth factor CTGF 16-14011 CTGF-1196- 14012 NM_001901.2 connective tissue growth factor CTGF 16-14012 CTGF-562-16- 14013 NM_001901.2 connective tissue growth factor CTGF 14013 CTGF-752-16- 14014 NM_001901.2 connective tissue growth factor CTGF 14014 CTGF-994-16- 14015 NM_001901.2 connective tissue growth factor CTGF 14015 CTGF-1040- 14016 NM_001901.2 connective tissue growth factor CTGF 16-14016 CTGF-1984- 14017 NM_001901.2 connective tissue growth factor CTGF 16-14017 CTGF-2195- 14018 NM_001901.2 connective tissue growth factor CTGF 16-14018 CTGF-2043- 14019 NM_001901.2 connective tissue growth factor CTGF 16-14019 CTGF-1892- 14020 NM_001901.2 connective tissue growth factor CTGF 16-14020 CTGF-1567- 14021 NM_001901.2 connective tissue growth factor CTGF 16-14021 CTGF-1780- 14022 NM_001901.2 connective tissue growth factor CTGF 16-14022 CTGF-2162- 14023 NM_001901.2 connective tissue growth factor CTGF 16-14023 CTGF-1034- 14024 NM_001901.2 connective tissue growth factor CTGF 16-14024 CTGF-2264- 14025 NM_001901.2 connective tissue growth factor CTGF 16-14025 CTGF-1032- 14026 NM_001901.2 connective tissue growth factor CTGF 16-14026 CTGF-1535- 14027 NM_001901.2 connective tissue growth factor CTGF 16-14027 CTGF-1694- 14028 NM_001901.2 connective tissue growth factor CTGF 16-14028 CTGF-1588- 14029 NM_001901.2 connective tissue growth factor CTGF 16-14029 CTGF-928-16- 14030 NM_001901.2 connective tissue growth factor CTGF 14030 CTGF-1133- 14031 NM_001901.2 connective tissue growth factor CTGF 16-14031 CTGF-912-16- 14032 NM_001901.2 connective tissue growth factor CTGF 14032 CTGF-753-16- 14033 NM_001901.2 connective tissue growth factor CTGF 14033 CTGF-918-16- 14034 NM_001901.2 connective tissue growth factor CTGF 14034 CTGF-744-16- 14035 NM_001901.2 connective tissue growth factor CTGF 14035 CTGF-466-16- 14036 NM_001901.2 connective tissue growth factor CTGF 14036 CTGF-917-16- 14037 NM_001901.2 connective tissue growth factor CTGF 14037 CTGF-1038- 14038 NM_001901.2 connective tissue growth factor CTGF 16-14038 CTGF-1048- 14039 NM_001901.2 connective tissue growth factor CTGF 16-14039 CTGF-1235- 14040 NM_001901.2 connective tissue growth factor CTGF 16-14040 CTGF-868-16- 14041 NM_001901.2 connective tissue growth factor CTGF 14041 CTGF-1131- 14042 NM_001901.2 connective tissue growth factor CTGF 16-14042 CTGF-1043- 14043 NM_001901.2 connective tissue growth factor CTGF 16-14043 CTGF-751-16- 14044 NM_001901.2 connective tissue growth factor CTGF 14044 CTGF-1227- 14045 NM_001901.2 connective tissue growth factor CTGF 16-14045 CTGF-867-16- 14046 NM_001901.2 connective tissue growth factor CTGF 14046 CTGF-1128- 14047 NM_001901.2 connective tissue growth factor CTGF 16-14047 CTGF-756-16- 14048 NM_001901.2 connective tissue growth factor CTGF 14048 CTGF-1234- 14049 NM_001901.2 connective tissue growth factor CTGF 16-14049 CTGF-916-16- 14050 NM_001901.2 connective tissue growth factor CTGF 14050 CTGF-925-16- 14051 NM_001901.2 connective tissue growth factor CTGF 14051 CTGF-1225- 14052 NM_001901.2 connective tissue growth factor CTGF 16-14052 CTGF-445-16- 14053 NM_001901.2 connective tissue growth factor CTGF 14053 CTGF-446-16- 14054 NM_001901.2 connective tissue growth factor CTGF 14054 CTGF-913-16- 14055 NM_001901.2 connective tissue growth factor CTGF 14055 CTGF-997-16- 14056 NM_001901.2 connective tissue growth factor CTGF 14056 CTGF-277-16- 14057 NM_001901.2 connective tissue growth factor CTGF 14057 CTGF-1052- 14058 NM_001901.2 connective tissue growth factor CTGF 16-14058 CTGF-887-16- 14059 NM_001901.2 connective tissue growth factor CTGF 14059 CTGF-914-16- 14060 NM_001901.2 connective tissue growth factor CTGF 14060 CTGF-1039- 14061 NM_001901.2 connective tissue growth factor CTGF 16-14061 CTGF-754-16- 14062 NM_001901.2 connective tissue growth factor CTGF 14062 CTGF-1130- 14063 NM_001901.2 connective tissue growth factor CTGF 16-14063 CTGF-919-16- 14064 NM_001901.2 connective tissue growth factor CTGF 14064 CTGF-922-16- 14065 NM_001901.2 connective tissue growth factor CTGF 14065 CTGF-746-16- 14066 NM_001901.2 connective tissue growth factor CTGF 14066 CTGF-993-16- 14067 NM_001901.2 connective tissue growth factor CTGF 14067 CTGF-825-16- 14068 NM_001901.2 connective tissue growth factor CTGF 14068 CTGF-926-16- 14069 NM_001901.2 connective tissue growth factor CTGF 14069 CTGF-923-16- 14070 NM_001901.2 connective tissue growth factor CTGF 14070 CTGF-866-16- 14071 NM_001901.2 connective tissue growth factor CTGF 14071 CTGF-563-16- 14072 NM_001901.2 connective tissue growth factor CTGF 14072 CTGF-823-16- 14073 NM_001901.2 connective tissue growth factor CTGF 14073 CTGF-1233- 14074 NM_001901.2 connective tissue growth factor CTGF 16-14074 CTGF-924-16- 14075 NM_001901.2 connective tissue growth factor CTGF 14075 CTGF-921-16- 14076 NM_001901.2 connective tissue growth factor CTGF 14076 CTGF-443-16- 14077 NM_001901.2 connective tissue growth factor CTGF 14077 CTGF-1041- 14078 NM_001901.2 connective tissue growth factor CTGF 16-14078 CTGF-1042- 14079 NM_001901.2 connective tissue growth factor CTGF 16-14079 CTGF-755-16- 14080 NM_001901.2 connective tissue growth factor CTGF 14080 CTGF-467-16- 14081 NM_001901.2 connective tissue growth factor CTGF 14081 CTGF-995-16- 14082 NM_001901.2 connective tissue growth factor CTGF 14082 CTGF-927-16- 14083 NM_001901.2 connective tissue growth factor CTGF 14083 SPP1-1091- 14131 NM_000582.2 Osteopontin SPP1 16-14131 PPIB--16- 14188 NM_000942 peptidylprolyl isomerase B (cyclophilin B) PPIB 14188 PPIB--17- 14189 NM_000942 peptidylprolyl isomerase B (cyclophilin B) PPIB 14189 PPIB--18- 14190 NM_000942 peptidylprolyl isomerase B (cyclophilin B) PPIB 14190 pGL3-1172- 14386 U47296 Cloning vector pGL3-Control pGL3 16-14386 pGL3-1172- 14387 U47296 Cloning vector pGL3-Control pGL3 16-14387 MAP4K4-2931- 14390 NM_004834 Mitogen-Activated Protein Kinase Kinase Kinase Kinase 4 MAP4K4 25-14390 (MAP4K4), transcript variant 1 miR-122--23- 14391 miR-122 14391 14084 NM_000582.2 Osteopontin SPP1 14085 NM_000582.2 Osteopontin SPP1 14086 NM_000582.2 Osteopontin SPP1 14087 NM_000582.2 Osteopontin SPP1 14088 NM_000582.2 Osteopontin SPP1 14089 NM_000582.2 Osteopontin SPP1 14090 NM_000582.2 Osteopontin SPP1 14091 NM_000582.2 Osteopontin SPP1 14092 NM_000582.2 Osteopontin SPP1 14093 NM_000582.2 Osteopontin SPP1 14094 NM_000582.2 Osteopontin SPP1 14095 NM_000582.2 Osteopontin SPP1 14096 NM_000582.2 Osteopontin SPP1 14097 NM_000582.2 Osteopontin SPP1 14098 NM_000582.2 Osteopontin SPP1 14099 NM_000582.2 Osteopontin SPP1 14100 NM_000582.2 Osteopontin SPP1 14101 NM_000582.2 Osteopontin SPP1 14102 NM_000582.2 Osteopontin SPP1 14103 NM_000582.2 Osteopontin SPP1 14104 NM_000582.2 Osteopontin SPP1 14105 NM_000582.2 Osteopontin SPP1 14106 NM_000582.2 Osteopontin SPP1 14107 NM_000582.2 Osteopontin SPP1 14108 NM_000582.2 Osteopontin SPP1 14109 NM_000582.2 Osteopontin SPP1 14110 NM_000582.2 Osteopontin SPP1 14111 NM_000582.2 Osteopontin SPP1 14112 NM_000582.2 Osteopontin SPP1 14113 NM_000582.2 Osteopontin SPP1 14114 NM_000582.2 Osteopontin SPP1 14115 NM_000582.2 Osteopontin SPP1 14116 NM_000582.2 Osteopontin SPP1 14117 NM_000582.2 Osteopontin SPP1 14118 NM_000582.2 Osteopontin SPP1 14119 NM_000582.2 Osteopontin SPP1 14120 NM_000582.2 Osteopontin SPP1 14121 NM_000582.2 Osteopontin SPP1 14122 NM_000582.2 Osteopontin SPP1 14123 NM_000582.2 Osteopontin SPP1 14124 NM_000582.2 Osteopontin SPP1 14125 NM_000582.2 Osteopontin SPP1 14126 NM_000582.2 Osteopontin SPP1 14127 NM_000582.2 Osteopontin SPP1 14128 NM_000582.2 Osteopontin SPP1 14129 NM_000582.2 Osteopontin SPP1 14130 NM_000582.2 Osteopontin SPP1 14132 NM_000582.2 Osteopontin SPP1 14133 NM_000582.2 Osteopontin SPP1 14134 NM_000582.2 Osteopontin SPP1 14135 NM_000582.2 Osteopontin SPP1 14136 NM_000582.2 Osteopontin SPP1 14137 NM_000582.2 Osteopontin SPP1 14138 NM_000582.2 Osteopontin SPP1 14139 NM_000582.2 Osteopontin SPP1 14140 NM_000582.2 Osteopontin SPP1 14141 NM_000582.2 Osteopontin SPP1 14142 NM_000582.2 Osteopontin SPP1 14143 NM_000582.2 Osteopontin SPP1 14144 NM_000582.2 Osteopontin SPP1 14145 NM_000582.2 Osteopontin SPP1 14146 NM_000582.2 Osteopontin SPP1 14147 NM_000582.2 Osteopontin SPP1 14148 NM_000582.2 Osteopontin SPP1 14149 NM_000582.2 Osteopontin SPP1 14150 NM_000582.2 Osteopontin SPP1 14151 NM_000582.2 Osteopontin SPP1 14152 NM_000582.2 Osteopontin SPP1 14153 NM_000582.2 Osteopontin SPP1 14154 NM_000582.2 Osteopontin SPP1 14155 NM_000582.2 Osteopontin SPP1 14156 NM_000582.2 Osteopontin SPP1 14157 NM_000582.2 Osteopontin SPP1 14158 NM_000582.2 Osteopontin SPP1 14159 NM_000582.2 Osteopontin SPP1 14160 NM_000582.2 Osteopontin SPP1 14161 NM_000582.2 Osteopontin SPP1 14162 NM_000582.2 Osteopontin SPP1 14163 NM_000582.2 Osteopontin SPP1 14164 NM_000582.2 Osteopontin SPP1 14165 NM_000582.2 Osteopontin SPP1 14166 NM_000582.2 Osteopontin SPP1 14167 NM_000582.2 Osteopontin SPP1 14168 NM_000582.2 Osteopontin SPP1 14169 NM_000582.2 Osteopontin SPP1 14170 NM_000582.2 Osteopontin SPP1 14171 NM_000582.2 Osteopontin SPP1 14172 NM_000582.2 Osteopontin SPP1 14173 NM_000582.2 Osteopontin SPP1 14174 NM_000582.2 Osteopontin SPP1 14175 NM_000582.2 Osteopontin SPP1 14176 NM_000582.2 Osteopontin SPP1 14177 NM_000582.2 Osteopontin SPP1 14178 NM_000582.2 Osteopontin SPP1 14179 NM_000582.2 Osteopontin SPP1 14180 NM_000582.2 Osteopontin SPP1 14181 NM_000582.2 Osteopontin SPP1 14182 NM_000582.2 Osteopontin SPP1 14183 NM_000582.2 Osteopontin SPP1 14184 NM_000582.2 Osteopontin SPP1 14185 NM_000582.2 Osteopontin SPP1 14186 NM_000582.2 Osteopontin SPP1 14187 NM_000582.2 Osteopontin SPP1

TABLE 2 Antisense backbone, chemistry, and sequence information. o: phosphodiester; s: phosphorothioate; P: 5′ phosphorylation; 0: 2′-OH; F: 2′-fluoro; m: 2′ O-methyl; +: LNA modification. Capital letters in the sequence signify ribonucleotides, lower case letters signify deoxyribonucleotides. Oligo SEQ ID Number Number AntiSense Backbone AntiSense Chemistry AntiSense Sequence ID NO: APOB- 12138 ooooooooooooooooooo 00000000000000000000m AUUGGUAUUCAGUGUGAUG   1 10167-20-12138 APOB- 12139 ooooooooooooooooooo 00000000000000000000m AUUCGUAUUGAGUCUGAUC   2 10167-20-12139 MAP4K4- 12266 2931-13-12266 MAP4K4- 12293 ooooooooooooooooooo Pf000fffff0f0000fff0 UAGACUUCCACAGAACUCU   3 2931-16-12293 MAP4K4- 12383 ooooooooooooooooooo 0000000000000000000 UAGACUUCCACAGAACUCU   4 2931-16-12383 MAP4K4- 12384 ooooooooooooooooooo P0000000000000000000 UAGACUUCCACAGAACUCU   5 2931-16-12384 MAP4K4- 12385 ooooooooooooooooooo Pf000fffff0f0000fff0 UAGACUUCCACAGAACUCU   6 3931-16-12385 MAP4K4- 12386 oooooooooosssssssso Pf000fffff0f0000fff0 UAGACUUCCACAGAACUCU   7 2931-16-12386 MAP4K4- 12387 oooooooooosssssssso P0000000000000000000 UAGACUUCCACAGAACUCU   8 2931-16-12387 MAP4K4- 12388 ooooooooooooooooo 00000000000000000 UAGACUUCCACAGAACU   9 2931-15-12388 MAP4K4- 12432 2931-13-12432 MAP4K4- 12266.2 2931-13-12266.2 APOB-- 12434 ooooooooooooooooooo 000000000000000000000 AUUGGUAUUCAGUGUGAUG  10 21-12434 oo m AC APOB-- 12435 ooooooooooooooooooo 000000000000000000000 AUUCGUAUUGAGUCUGAUC  11 21-12435 oo m AC MAP4K4- 12451 oooooooooosssssssso Pf000fffff0f0000ffmm UAGACUUCCACAGAACUCU  12 2931-16-12451 MAP4K4- 12452 oooooooooosssssssso Pf000fffff0f0000ffmm UAGACUUCCACAGAACUCU  13 2931-16-12452 MAP4K4- 12453 oooooooooosssssssso Pf000fffff0f0000ffmm UAGACUUCCACAGAACUCU  14 2931-16-12453 MAP4K4- 12454 oooooooooooosssssss Pm000fffff0f0000ffffm UAGACUUCCACAGAACUCU  15 2931-17-12454 so m UC MAP4K4- 12455 oooooooosssssssssss Pm000fffff0f0000ffffm UAGACUUCCACAGAACUCU  16 2931-17-12455 so m UC MAP4K4- 12456 oooooooooooosssssss Pm000fffff0f0000fffff UAGACUUCCACAGAACUCU  17 2931-19-12456 ssssso f00mm UCAAAG --27-12480 123480 --27-12481 12481 APOB- 12505 ooooooooooooooooooo 00000000000000000000m AUUGGUAUUCAGUGUGAUG  18 10167-21-12505 os AC APOB- 12506 ooooooooooooooooooo 00000000000000000000m AUUCGUAUUGAGUCUGAUC  19 10167-21-12506 os AC MAP4K4- 12539 ooooooooooossssssss Pf000fffff0f0000fff0 UAGACUUCCACAGAACUCU  20 2931-16-12539 APOB- 12505.2 ooooooooooooooooooo 00000000000000000000m AUUGGUAUUCAGUGUGAUG  21 10167-21-12505.2 oo AC APOB- 12506.2 ooooooooooooooooooo 00000000000000000000m AUUCGUAUUGAGUCUGAUC  22 10167-21-12506.2 oo AC MAP4K4-- 12565 13-12565 MAP4K4- 12386.2 oooooooooosssssssso Pf000fffff0f0000fff0 UAGACUUCCACAGAACUCU  23 2931-16-12386.2 MAP4K4- 12815 2931-13-12815 APOB--13-12957 12957 MAP4K4-- 12983 oooooooooooosssssso Pm000fffff0m0000mmm0 uagacuuccacagaacucu  24 16-12983 MAP4K4-- 12984 oooooooooooossssss Pm000fffff0m0000mmm0 uagacuuccacagaacucu  25 26-12984 MAP4K4-- 12985 oooooooooooosssssso Pm000fffff0m0000mmm0 uagacuuccacagaacucu  26 16-12985 MAP4K4-- 12986 oooooooooosssssssso Pf000fffff0f0000fff0 UAGACUUCCACAGAACUCU  27 16-12986 MAP4K4-- 12987 ooooooooooooossssss P0000f00ff0m0000m0m0 UagacUUccacagaacUcU  28 16-12987 MAP4K4-- 12983 ooooooooooooossssss P0000f00ff0m0000m0m0 UagacUUccacagaacUcu  29 16-12988 MAP4K4-- 12989 ooooooooooooossssss P0000ff0ff0m0000m0m0 UagacuUccacagaacUcu  30 16-12989 MAP4K4-- 12990 ooooooooooooossssss Pf0000ff000000000m00 uagaCuuCCaCagaaCuCu  31 16-12990 MAP4K4-- 12991 ooooooooooooossssss Pf0000fff00m00000mm0 uagaCuucCacagaaCucu  32 16-12991 MAP4K4-- 12992 ooooooooooooossssss Pf000fffff0000000m00 uagacuuccaCagaaCuCu  33 16-12992 MAP4K4-- 12993 ooooooooooooossssss P0000000000000000000 UagaCUUCCaCagaaCUCU  34 16-12993 MAP4K4-- 12994 ooooooooooooossssss P0000f0f0f0000000m00 UagacUuCcaCagaaCuCu  35 16-12994 MAP4K4-- 12995 oooooooooooosssssso Pf000fffff0000000000 uagacuuccaCagaaCUCU  36 16-12995 MAP4K4-- 13012 2931-19-13012 MAP4K4-- 13016 2931-19-13016 PPIB--13-13021 13021 pGL3- 13040 1172-13-13040 --16-13047 13047 oooooooooooossssss Pm000000000m0000mmm0 UAGACUUCCACAGAACUCU  37 SOD1- 13090 530-13-13090 SOD1- 13091 523-13-13091 SOD1- 13092 535-13-13092 SOD1- 13093 536-13-13093 SOD1- 13094 396-13-13094 SOD1- 13095 385-13-13095 SOD1- 13096 195-13-13096 APOB- 13115 4314-13-13115 APOB- 13116 3384-13-13116 APOB- 13117 3547-13-13117 APOB- 13118 4318-13-13118 APOB- 13119 3741-13-13119 PPIB--16-13136 13136 oooooooooooossssss Pm0fffff0f00mm000mm0 UGUUUUUGUAGCCAAAUCC  38 APOB- 13154 4314-15-13154 APOB- 13155 3547-15-13155 APOB- 13157 4318-15-13157 APOB- 13158 3741-15-13158 APOB--15-13159 13159 APOB--15-13160 13160 SOD1- 13163 oooooooooooosssssso Pm0ffffffff0mmmmm0m0 UACUUUCUUCAUUUCCACC  39 530-16-13163 SOD1- 13164 oooooooooooosssssso Pmff0fffff0fmmmm0mm0 UUCAUUUCCACCUUUGCCC  40 532-16-13164 SOD1- 13165 oooooooooooosssssso Pmfff0f0ffffmmmm0mm0 CUUUGUACUUUCUUCAUUU  41 535-16-13165 SOD1- 13166 oooooooooooosssssso Pmffff0f0fffmmmmm0m0 UCUUUGUACUUUCUUCAUU  42 536-16-13166 SOD1- 13167 oooooooooooosssssso Pmf00f00ff0f0mm0mmm0 UCAGCAGUCACAUUGCCCA  43 396-16-13167 SOD1- 13168 oooooooooooosssssso Pmff0fff000fmmmm00m0 AUUGCCCAAGUCUCCAACA  44 385-16-13168 SOD1- 13169 oooooooooooosssssso Pmfff0fff0000mm00m00 UUCUGCUCGAAAUUGAUGA  45 195-16-13169 pGL3- 13170 oooooooooooosssssso Pm00ff0f0ffm0ff00mm0 AAAUCGUAUUUGUCAAUCA  46 1172-16-13170 pGL3- 13171 ooooooooooooossssss Pm00ff0f0ffm0ff00mm0 AAAUCGUAUUUGUCAAUCA  47 1172-16-13171 MAP4K4- 13189 ooooooooooooooooooo 0000000000000000000 UAGACUUCCACAGAACUCU  48 2931-19-13189 CTGF- 13190 1222-13-13190 CTGF- 13192 813-13-13192 CTGF- 13194 747-13-13194 CTGF- 13196 817-13-13196 CTGF- 13198 1174-13-13198 CTGF- 13200 1005-13-13200 CTGF- 13202 814-13-13202 CTGF- 13204 816-13-13204 CTGF- 13206 1001-13-13206 CTGF- 13208 1173-13-13208 CTGF- 13210 749-13-13210 CTGF- 13212 792-13-13212 CTGF- 13214 1162-13-13214 CTGF- 13216 811-13-13216 CTGF- 13218 797-13-13218 CTGF- 13220 1175-13-13220 CTGF- 13222 1172-13-13200 CTGF- 13224 1177-13-13224 CTGF- 13226 1176-13-13226 CTGF- 13228 812-13-13228 CTGF- 13230 745-13-13230 CTGF- 13232 1230-13-13232 CTGF- 13234 920-13-13234 CTGF- 13236 679-13-13236 CTGF- 13238 992-13-13238 CTGF- 13240 1045-13-13240 CTGF- 13242 1231-13-13242 CTGF- 13244 991-13-13244 CTGF- 13246 998-13-13246 CTGF- 13248 1049-13-13200 CTGF- 13250 1044-13-13250 CTGF- 13252 1327-13-13252 CTGF- 13254 1196-13-13254 CTGF- 13256 562-13-13256 CTGF- 13258 752-13-13258 CTGF- 13260 994-13-13260 CTGF- 13262 1040-13-13262 CTGF- 13264 1984-13-13264 CTGF- 13266 2195-13-13266 CTGF- 13268 2043-13-13268 CTGF- 13270 1892-13-13270 CTGF- 13272 1567-13-13272 CTGF- 13274 1780-13-13274 CTGF- 13276 2162-13-13276 CTGF- 13278 1034-13-13278 CTGF- 13280 2264-13-13280 CTGF- 13282 1032-13-13282 CTGF- 13284 1535-13-13284 CTGF- 13286 1694-13-13286 CTGF- 13288 1588-13-13288 CTGF- 13290 928-13-13290 CTGF- 13292 1133-13-13292 CTGF- 13294 912-13-13294 CTGF- 13296 753-13-13296 CTGF- 13298 918-13-13298 CTGF- 13230 744-13-13230 CTGF- 13202 466-13-13202 CTGF- 13204 917-13-13204 CTGF- 13206 1038-13-13206 CTGF- 13208 1048-13-13208 CTGF- 13310 1235-13-13310 CTGF- 13312 868-13-13312 CTGF- 13314 1131-13-13314 CTGF- 13316 1043-13-13316 CTGF- 13318 751-13-13318 CTGF- 13320 1227-13-13320 CTGF- 13322 867-13-13322 CTGF- 13324 1128-13-13324 CTGF- 13326 756-13-13326 CTGF- 13328 1234-13-13328 CTGF- 13330 916-13-13330 CTGF- 13332 925-13-13332 CTGF- 13334 1225-13-13334 CTGF- 13336 445-13-13336 CTGF- 13338 446-13-13338 CTGF- 13340 913-13-13340 CTGF- 13342 997-13-13342 CTGF- 13344 277-13-13344 CTGF- 13346 1052-13-13346 CTGF- 13348 887-13-13348 CTGF- 13350 914-13-13350 CTGF- 13352 1039-13-13352 CTGF- 13354 754-13-13354 CTGF- 13356 1130-13-13356 CTGF- 13358 919-13-13358 CTGF- 13360 922-13-13360 CTGF- 13362 746-13-13362 CTGF- 13364 993-13-13364 CTGF- 13366 825-13-13366 CTGF- 13368 926-13-13368 CTGF- 13370 923-13-13370 CTGF- 13372 866-13-13372 CTGF- 13374 563-13-13374 CTGF- 13376 823-13-13376 CTGF- 13378 1233-13-13378 CTGF- 13380 924-13-13380 CTGF- 13382 924-13-13382 CTGF- 13384 443-13-13384 CTGF- 13386 1041-13-13386 CTGF- 13388 1042-13-13388 CTGF- 13390 755-13-13390 CTGF- 13392 467-13-13392 CTGF- 13394 995-13-13394 CTGF- 13396 927-13-13396 SPP1- 13398 1025-13-13398 SPP1- 13400 1049-13-13400 SPP1- 13402 1051-13-13402 SPP1- 13404 1048-13-13404 SPP1- 13406 1050-13-13406 SPP1- 13408 1047-13-13408 SPP1- 13410 800-13-13410 SPP1- 13412 492-13-13412 SPP1- 13414 612-13-13414 SPP1- 13416 481-13-13416 SPP1- 13418 614-13-13418 SPP1- 13420 951-13-13420 SPP1- 13422 482-13-13422 SPP1- 13424 856-13-13424 SPP1- 13426 857-13-13426 SPP1- 13428 365-13-13428 SPP1- 13430 359-13-13430 SPP1- 13432 357-13-13432 SPP1- 13434 858-13-13434 SPP1- 13436 1012-13-13436 SPP1- 13438 1014-13-13438 SPP1- 13440 356-13-13440 SPP1- 13442 368-13-13442 SPP1- 13444 1011-13-13444 SPP1- 13446 754-13-13446 SPP1- 13448 1021-13-13448 SPP1- 13450 1330-13-13450 SPP1- 13452 346-13-13452 SPP1- 13454 869-13-13454 SPP1- 13456 701-13-13456 SPP1- 13458 896-13-13458 SPP1- 13460 1035-13-13460 SPP1- 13462 1170-13-13462 SPP1- 13464 1282-13-13464 SPP1- 13466 1537-13-13466 SPP1- 13468 692-13-13468 SPP1- 13470 840-13-13470 SPP1- 13472 1163-13-13472 SPP1- 13474 789-13-13474 SPP1- 13476 841-13-13476 SPP1- 13478 852-13-13478 SPP1- 13480 209-13-13480 SPP1- 13482 1276-13-13482 SPP1- 13484 137-13-13484 SPP1- 13486 711-13-13486 SPP1- 13488 582-13-13488 SPP1- 13490 839-13-13490 SPP1- 13492 1091-13-13492 SPP1- 13494 884-13-13494 SPP1- 13496 903-13-13496 SPP1- 13498 1090-13-13498 SPP1- 13500 474-13-13500 SPP1- 13502 575-13-13502 SPP1- 13504 671-13-13504 SPP1- 13506 924-13-13506 SPP1- 13508 1185-13-13508 SPP1- 13510 1221-13-13510 SPP1- 13512 347-13-13512 SPP1- 13514 634-13-13514 SPP1- 13516 877-13-13516 SPP1- 13518 1033-13-13518 SPP1- 13520 714-13-13520 SPP1- 13522 791-13-13522 SPP1- 13524 813-13-13524 SPP1- 13526 939-13-13526 SPP1- 13528 1161-13-13528 SPP1- 13530 1164-13-13530 SPP1- 13532 1190-13-13532 SPP1- 13534 1333-13-13534 SPP1- 13536 537-13-13536 SPP1- 13538 684-13-13538 SPP1- 13540 707-13-13540 SPP1- 13542 799-13-13542 SPP1- 13544 853-13-13544 SPP1- 13546 888-13-13546 SPP1- 13548 1194-13-13548 SPP1- 13550 1279-13-13550 SPP1- 13552 1300-13-13552 SPP1- 13554 1510-13-13554 SPP1- 13556 1543-13-13556 SPP1- 13558 434-13-13558 SPP1- 13560 600-13-13560 SPP1- 13562 863-13-13562 SPP1- 13564 902-13-13564 SPP1- 13566 921-13-13566 SPP1- 13568 154-13-13568 SPP1- 13570 217-13-13570 SPP1- 13572 816-13-13572 SPP1- 13574 882-13-13574 SPP1- 13576 932-13-13576 SPP1- 13578 1509-13-13578 SPP1- 13580 157-13-13580 SPP1- 13582 350-13-13582 SPP1- 13584 511-13-13584 SPP1- 13586 605-13-13586 SPP1- 13588 811-13-13588 SPP1- 13590 892-13-13590 SPP1- 13592 922-13-13592 SPP1- 13594 1169-13-13594 SPP1- 13596 1182-13-13596 SPP1- 13598 1539-13-13598 SPP1- 13600 1541-13-13600 SPP1- 13602 427-13-13602 SPP1- 13604 533-13-13504 APOB--13-13763 13763 APOB--13-13764 13764 MAP4K4-- 13766 oooooooooooosssssso Pm000fffff0m0000mmm0 UAGACUUCCACAGAACUCU  49 16-13766 PPIB--13-13767 13767 PPIB--15-13768 13768 PPIB-17-13769 13769 MAP4K4-- 13939 oooooooooooosssssso m000f0ffff0m0m00m0m UAGACAUCCUACACAGCAC  50 16-13939 APOB- 13940 oooooooooooosssssso Pm0fffffff000mmmmm00 UGUUUCUCCAGAUCCUUGC  51 4314-16-13940 APOB- 13941 oooooooooooosssssso Pm0fffffff000mmmmm00 UGUUUCUCCAGAUCCUUGC  52 4314-17-13941 APOB--16-13942 13942 oooooooooooosssssso Pm00f000f000mmm0mmm0 UAGCAGAUGAGUCCAUUUG  53 APOB--18-13943 13943 oooooooooooooooosss Pm00f000f000mmm0mmm00 UAGCAGAUGAGUCCAUUUG  54 ssso 000 GAGA APOB--17-13944 13944 oooooooooooosssssso Pm00f000f000mmm0mmm0 UAGCAGAUGAGUCCAUUUG  55 APOB--19-13945 13945 oooooooooooooooosss Pm00f000f000mmm0mmm00 UAGCAGAUGAGUCCAUUUG  56 ssso 000 GAGA APOB- 13946 oooooooooooosssssso Pmf0ff0ffffmmm000mm0 AUGUUGUUUCUCCAGAUCC  57 4314-16-13946 APOB- 13947 oooooooooooosssssso Pmf0ff0ffffmmm000mm0 AUGUUGUUUCUCCAGAUCC  58 4314-17-13947 APOB--16-14948 13948 oooooooooooosssssso Pm0fff000000mmmm0m00 UGUUUGAGGGACUCUGUGA  59 APOB--17-13949 13949 oooooooooooosssssso Pm0fff000000mmmm0m00 UGUUUGAGGGACUCUGUGA  60 APOB--16-13950 13950 oooooooooooosssssso Pmff00f0fff00m0m00m0 AUUGGUAUUCAGUGUGAUG  61 APOB--18-13951 13951 oooooooooooooooosss Pmff00f0fff00m0m00m00 AUUGGUAUUCAGUGUGAUG  62 ssso m00 ACAC APOB--17-13952 13952 oooooooooooosssssso Pmff00f0fff00m0m00m0 AUUGGUAUUCAGUGUGAUG  63 APOB--19-13953 13953 oooooooooooooooosss Pmff00f0fff00m0m00m00 AUUGGUAUUCAGUGUGAUG  64 ssso m00 ACAC MAP4K4-- 13766.2 oooooooooooosssssso Pm000fffff0m0000mmm0 UAGACUUCCACAGAACUCU  65 16-13766.2 CTGF- 13980 oooooooooooosssssso Pm0f0ffffffm0m00m0m0 UACAUCUUCCUGUAGUACA  66 1222-16-13980 CTGF- 13981 oooooooooooosssssso Pm0f0ffff0mmmm0m000 AGGCGCUCCACUCUGUGGU  67 813-16-13981 CTGF- 13982 oooooooooooosssssso Pm0ffffff00mm0m0000 UGUCUUCCAGUCGGUAAGC  68 747-16-13982 CTGF- 13983 oooooooooooosssssso Pm00f000f0fmmm0mmmm0 GAACAGGCGCUCCACUCUG  69 817-16-13983 CTGF- 13984 oooooooooooosssssso Pm00ff0f00f00m000m00 CAGUUGUAAUGGCAGGCAC  70 1174-16-13984 CTGF- 13985 oooooooooooosssssso Pmff000000mmm000mm0 AGCCAGAAAGCUCAAACUU  71 1005-16-13985 CTGF- 13986 oooooooooooosssssso Pm000f0ffff0mmmm0m00 CAGGCGCUCCACUCUGUGG  72 814-16-13986 CTGF- 13987 oooooooooooosssssso Pm0f000f0ffmm0mmmm00 AACAGGCGCUCCACUCUGU  73 816-16-13987 CTGF- 13988 oooooooooooosssssso Pm0000fff000mmm00m0 AGAAAGCUCAAACUUGAUA  74 1001-16-13988 CTGF- 13989 oooooooooooosssssso Pmff0f00f00m000m0m0 AGUUGUAAUGGCAGGCACA  75 1173-16-13989 CTGF- 13990 oooooooooooosssssso Pmf0ffffff00mm00m00 CGUGUCUUCCAGUCGGUAA  76 749-16-13990 CTGF- 13991 oooooooooooosssssso Pm00ff000f00mm00mmm0 GGACCAGGCAGUUGGCUCU  77 792-16-13991 CTGF- 13992 oooooooooooosssssso Pm000f0f000mmmm00m00 CAGGCACAGGUCUUGAUGA  78 1162-16-13992 CTGF- 13993 oooooooooooosssssso Pmf0ffff0ffmm0m00mm0 GCGCUCCACUCUGUGGUCU  79 811-16-13993 CTGF- 13994 oooooooooooosssssso Pm0fff000ff000m00mm0 GGUCUGGACCAGGCAGUUG  80 797-16-13994 CTGF- 13995 oooooooooooosssssso Pmf00ff0f00m00m000m0 ACAGUUGUAAUGGCAGGCA  81 1175-16-13995 CTGF- 13996 oooooooooooosssssso Pmff0f00f00m000m0m00 GUUGUAAUGGCAGGCACAG  82 1172-16-13996 CTGF- 13997 oooooooooooosssssso Pm00f00ff0f00m00m000 GGACAGUUGUAAUGGCAGG  83 1177-16-13997 CTGF- 13998 oooooooooooosssssso Pm0f0ffff0fmmm0m00m0 GGCGCUCCACUCUGUGGUC  84 1176-16-13998 CTGF- 13999 oooooooooooosssssso Pm0f0ffff0fmmm0m00m0 GGCGCUCCACUCUGUGGUC  85 812-16-13999 CTGF- 14000 oooooooooooosssssso Pmfffff00ff00m000mm0 UCUUCCAGUCGGUAAGCCG  86 745-16-14000 CTGF- 14001 oooooooooooosssssso Pm0fffff0f0m0mmmmmm0 UGUCUCCGUACAUCUUCCU  87 1230-16-14001 CTGF- 14002 oooooooooooosssssso Pmffff-f0000mmm00m0 AGCUUCGCAAGGCCUGACC  88 920-16-14002 CTGF- 14003 oooooooooooosssssso Pm0ffffff0f00m0mmmm0 CACUCCUCGCAGCAUUUCC  89 679-16-14003 CTGF- 14004 oooooooooooosssssso Pm00fff00f000mmm0000 AAACUUGAUAGGCUUGGAG  90 992-16-14004 CTGF- 14005 oooooooooooosssssso Pmffff0f0000mmm00mm0 ACUCCACAGAAUUUAGCUC  91 1045-16-14005 CTGF- 14006 oooooooooooosssssso Pmf0fffff0f0m0mmmmm0 AUGUCUCCGUACAUCUUCC  92 1231-16-14006 CTGF- 14007 oooooooooooosssssso Pm0fff00f000mmm00000 AACUUGAUAGGCUUGGAGA  93 991-16-14007 CTGF- 14008 oooooooooooosssssso Pm00fff000fmm00m0000 AAGCUCAAACUUGAUAGGC  94 998-16-14008 CTGF- 14009 oooooooooooosssssso Pmf0f0ffff0m0000mmm0 ACAUACUCCACAGAAUUUA  95 1049-16-14009 CTGF- 14010 oooooooooooosssssso Pmfff0f0000mmm00mmm0 CUCCACAGAAUUUAGCUCG  96 1044-16-14010 CTGF- 14011 oooooooooooosssssso Pm0f0ff0ff0000mm0mm0 UGUGCUACUGAAAUCAUUU  97 1327-16-14011 CTGF- 14012 oooooooooooosssssso Pm0000f0ff0mm0mmmmm0 AAAGAUGUCAUUGUCUCCG  98 1196-16-14012 CTGF- 14013 oooooooooooosssssso Pmf0f0ff00f0mmm0m000 GUGCACUGGUACUUGCAGC  99 562-16-14013 CTGF- 14014 oooooooooooosssssso Pm00f0f0fffmmm00mm00 AAACGUGUCUUCCAGUCGG 100 752-16-14014 CTGF- 14015 oooooooooooosssssso Pmf000fff00m000mmm00 UCAAACUUGAUAGGCUUGG 101 994-16-14015 CTGF- 14016 oooooooooooosssssso Pmf0000fff00mmm00m00 ACAGAAUUUAGCUCGGUAU 102 1040-16-14016 CTGF- 14017 oooooooooooosssssso Pmf0f0ffff0mmm0m00m0 UUACAUUCUACCUAUGGUG 103 1984-16-14017 CTGF- 14018 oooooooooooosssssso Pm00ff00ff00mM0m0m00 AAACUGAUCAGCUAUAUAG 104 2195-16-14018 CTGF- 14019 oooooooooooosssssso Pm0fff000f0000mmmmm0 UAUCUGAGCAGAAUUUCCA 105 2043-16-14019 CTGF- 14020 oooooooooooosssssso Pmf00fff000m00mm0m00 UUAACUUAGAUAACUGUAC 106 1892-16-14020 CTGF- 14021 oooooooooooosssssso Pm0ff0fff0f0m0000m00 UAUUACUCGUAUAAGAUGC 107 1567-16-14021 CTGF- 14022 oooooooooooosssssso Pm00ff0fff00mmm00mm0 AAGCUGUCCAGUCUAAUCG 108 1780-16-14022 CTGF- 14023 oooooooooooosssssso Pm00F00000Fm0mmm0mm0 UAAUAAAGGCCAUUUGUUC 109 2162-16-14023 CTGF- 14024 oooooooooooosssssso Pmff00fff00m0m0mmmm0 UUUAGCUCGGUAUGUCUUC 110 1034-16-14024 CTGF- 14025 oooooooooooosssssso Pmf0fffff00m000m0000 ACACUCUCAACAAAUAAAC 111 2264-16-14025 CTGF- 14026 oooooooooooosssssso Pm00fff00f0m0mmmmm00 UAGCUCGGUAUGUCUUCAU 112 1032-16-14026 CTGF- 14027 oooooooooooosssssso Pm00fffffff0mm00m0m0 UAACCUUUCUGCUGGUACC 113 1535-16-14027 CTGF- 14028 oooooooooooosssssso Pmf000000f00mmm00mm0 UUAAGGAACAACUUGACUC 114 1694-16-14028 CTGF- 14029 oooooooooooosssssso Pmf0f0ffff000m00m000 UUACACUUCAAAUAGCAGG 115 1588-16-14029 CTGF- 14030 oooooooooooosssssso Pmff000ff00mmmm0m000 UCCAGGUCAGCUUCGCAAG 116 928-16-14030 CTGF- 14031 oooooooooooosssssso Pmffffff0f00mmmm0mm0 CUUCUUCAUGACCUCGCCG 117 1133-16-14031 CTGF- 14032 oooooooooooosssssso Pm000fff00fm0m0m0m00 AAGGCCUGACCAUGCACAG 118 912-16-14032 CTGF- 14033 oooooooooooosssssso Pm000f0f0ffmmmm00mm0 CAAACGUGUCUUCCAGUCG 119 753-16-14033 CTGF- 14034 oooooooooooosssssso Pmfff0f0000mmm00mm00 CUUCGCAAGGCCUGACCAU 120 918-16-14034 CTGF- 14035 oooooooooooosssssso pmffff00ff00m000mm00 CUUCCAGUCGGUAAGCCGC 121 744-16-14035 CTGF- 14036 oooooooooooosssssso Pmf00ffff0f00mm00mm0 CCGAUCUUGCGGUUGGCCG 122 466-16-14036 CTGF- 14037 oooooooooooosssssso Pmff0f0000fmm00mm0m0 UUCGCAAGGCCUGACCAUG 123 917-16-14037 CTGF- 14038 oooooooooooosssssso Pm00fff00fmm0m0m00 AGAAUUUAGCUCGGUAUGU 124 1038-16-14038 CTGF- 14039 oooooooooooosssssso Pm0f0ffff0f0000mmm00 CAUACUCCACAGAAUUUAG 125 1048-16-14039 CTGF- 14040 oooooooooooosssssso Pm0ff0f0fffmmm0m0m0 UGCCAUGUCUCCGUACAUC 126 1235-16-14040 CTGF- 14041 oooooooooooosssssso Pm000f0ff0fm0mm00m00 GAGGCGUUGUCAUUGGUAA 127 868-16-14041 CTGF- 14042 oooooooooooosssssso Pmffff0f00fmmm0mm0m0 UCUUCAUGACCUCGCCGUC 128 1131-16-14042 CTGF- 14043 oooooooooooosssssso Pmff0f0000fmm00mmm00 UCCACAGAAUUUAGCUCGG 129 1043-16-14043 CTGF- 14044 oooooooooooosssssso Pm0f0f0ffffmm00mm000 AACGUGUCUUCCAGUCGGU 130 751-16-14044 CTGF- 14045 oooooooooooosssssso Pmfff0f0f0fmmmmmm0m0 CUCCGUACAUCUUCCUGUA 131 1227-16-14045 CTGF- 14046 oooooooooooosssssso Pm0f0ff0ff0mm00m000 AGGCGUUGUCAUUGGUAAC 132 867-16-14046 CTGF- 14047 oooooooooooosssssso Pmf0f00ffff0mm0mm000 UCAUGACCUCGCCGUCAGG 133 1128-16-14047 CTGF- 14048 oooooooooooosssssso Pm0ff000f0f0mmmmmm00 GGCCAAACGUGUCUUCCAG 134 756-16-14048 CTGF- 14049 oooooooooooosssssso Pmff0f0ffffmm0m0mm0 GCCAUGUCUCCGUACAUCU 135 1234-16-14049 CTGF- 14050 oooooooooooosssssso Pmf0f0000ffm00mm0m00 UCGCAAGGCCUGACCAUGC 136 916-16-14050 CTGF- 14051 oooooooooooosssssso Pm0ff00fffmm0000m0 AGGUCAGCUUCGCAAGGCC 137 925-16-14051 CTGF- 14052 oooooooooooosssssso Pmf0f0f0fffmmmm0m000 CCGUACAUCUUCCUGUAGU 138 1225-16-14052 CTGF- 14053 oooooooooooosssssso Pm00ff0000fm0m000000 GAGCCGAAGUCACAGAAGA 139 445-16-14053 CTGF- 14054 oooooooooooosssssso Pm000ff0000mm0m00000 GGAGCCGAAGUCACAGAAG 140 446-16-14054 CTGF- 14055 oooooooooooosssssso Pm0000fff00mm0m0m0m0 CAAGGCCUGACCAUGCACA 141 913-16-14055 CTGF- 14056 oooooooooooosssssso Pmfff000ffm00m000m0 AGCUCAAACUUGAUAGGCU 142 997-16-14056 CTGF- 14057 oooooooooooosssssso Pmf0f00ffff00mm00m00 CUGCAGUUCUGGCCGACGG 143 277-16-14057 CTGF- 14058 oooooooooooosssssso Pm0f0f0f0ffmm0m00000 GGUACAUACUCCACAGAAU 144 1052-16-14058 CTGF- 14059 oooooooooooosssssso Pmf0fffffff00mmm0m00 CUGCUUCUCUAGCCUGCAG 145 887-16-14050 CTGF- 14060 oooooooooooosssssso Pmf0000fff00mm0m0m00 GCAAGGCCUGACCAUGCAC 146 914-16-14060 CTGF- 14061 oooooooooooosssssso Pm0000fff00mmm00m0m0 CAGAAUUUAGCUCGGUAUG 147 1039-16-14061 CTGF- 14062 oooooooooooosssssso Pmf000f0f0fmmmmm00m0 CCAAACGUGUCUUCCAGUC 148 754-16-14062 CTGF- 14063 oooooooooooosssssso Pmfff0f00ffmmmm0mm0 CUUCAUGACCUCGCCGUCA 149 1130-16-14063 CTGF- 14064 oooooooooooosssssso Pmffff0f0000mmm00mm0 GCUUCGCAAGGCCUGACCA 150 919-16-14064 CTGF- 14065 oooooooooooosssssso Pmf00ffff0f0000mmm00 UCAGCUUCGCAAGGCCUGA 151 922-16-14065 CTGF- 14066 oooooooooooosssssso Pmffffff00fm0m000m0 GUCUUCCAGUCGGUAAGCC 152 746-16-14066 CTGF- 14067 oooooooooooosssssso Pm000fff00f000mmm000 CAAACUUGAUAGGCUUGGA 153 993-16-14067 CTGF- 14068 oooooooooooosssssso Pm0ffff0000m000m0m0 AGGUCUUGGAACAGGCGCU 154 825-16-14068 CTGF- 14069 oooooooooooosssssso Pm000ff00ffmmm00000 CAGGUCAGCUUCGCAAGGC 155 926-16-14069 CTGF- 14070 oooooooooooosssssso Pmff00ffff0m0000mmm0 GUCAGCUUCGCAAGGCCUG 156 923-16-14070 CTGF- 14071 oooooooooooosssssso Pm0f0ff0ff0mm00m00m0 GGCGUUGUCAUUGGUAACC 157 866-16-14071 CTGF- 14072 oooooooooooosssssso Pmf0f0ff00m0mmm0m00 CGUGCACUGGUACUUGCAG 158 563-16-14072 CTGF- 14073 oooooooooooosssssso Pmffff0000f000m0mmm0 GUCUUGGAACAGGCGCUCC 159 823-16-14073 CTGF- 14074 oooooooooooosssssso Pmf0f0fffff0m0m0mmm0 CCAUGUCUCCGUACAUCUU 160 1233-16-14074 CTGF- 14075 oooooooooooosssssso Pm0ff00ffff0m0000mm0 GGUCAGCUUCGCAAGGCCU 161 924-16-14075 CTGF- 14076 oooooooooooosssssso Pm00ffff0f0000mmm000 CAGCUUCGCAAGGCCUGAC 162 921-16-14076 CTGF- 14077 oooooooooooosssssso Pmff0000ff0m00000000 GCCGAAGUCACAGAAGAGG 163 443-16-14077 CTGF- 14078 oooooooooooosssssso Pm0f0000fff00mmm00m0 CACAGAAUUUAGCUCGGUA 164 1041-16-14078 CTGF- 14079 oooooooooooosssssso Pmf0f0000ffm00mmm000 CCACAGAAUUUAGCUCGGU 165 1042-16-14079 CTGF- 14080 oooooooooooosssssso Pmff000f0f0mmmmmm000 GCCAAACGUGUCUUCCAGU 166 755-16-14080 CTGF- 14081 oooooooooooosssssso Pmf0f00ffff0m0mm00m0 GCCGAUCUUGCGGUUGGCC 167 467-16-14081 CTGF- 14082 oooooooooooosssssso Pmff000fff00m000mmm0 CUCAAACUUGAUAGGCUUG 168 995-16-14082 CTGF- 14083 oooooooooooosssssso Pmf000ff00fmmm0m0000 CCAGGUCAGCUUCGCAAGG 169 927-16-14083 SPP1- 14131 oooooooooooosssssso Pmff00ff000m0m0000m0 UUUGACUAAAUGCAAAGUG 170 1091-16-14131 PPIB--16-14188 14188 ooooooooooooossssss Pm0fffff0f00mm000mm0 UGUUUUUGUAGCCAAAUCC 171 PPIB--17-14189 14189 ooooooooooooossssss Pm0fffff0f00mm000mm0 UGUUUUUGUAGCCAAAUCC 172 PPIB--18-14190 14190 ooooooooooooossssss Pm0fffff0f00mm000mm0 UGUUUUUGUAGCCAAAUCC 173 pGL3- 14386 oooooooooooosssssso Pm00ff0f0ffm0mm00mm0 AAAUCGUAUUUGUCAAUCA 174 1172-16-14386 pGL3- 14387 oooooooooooosssssso Pm00ff0f0ffm0mm00mm0 AAAUCGUAUUUGUCAAUCA 175 1172-16-14387 MAP4K4- 14390 2931-25-14390 miR-122-- 14391 23-14391 14084 oooooooooooosssssso Pmff00fff0f000000m00 UCUAAUUCAUGAGAAAUAC 616 14085 oooooooooooosssssso Pm00ff00fffm000000m0 UAAUUGACCUCAGAAGAUG 617 14086 oooooooooooosssssso Pmff00ff00fmmm000000 UUUAAUUGACCUCAGAAGA 618 14087 oooooooooooosssssso Pm0ff00ffff000000m00 AAUUGACCUCAGAAGAUGC 619 14088 oooooooooooosssssso Pmf00ff00ffmm0000000 UUAAUUGACCUCAGAAGAU 620 14089 oooooooooooosssssso Pmff00ffff000000m0m0 AUUGACCUCAGAAGAUGCA 621 14090 oooooooooooosssssso Pmf0fff00ff00mmm0mm0 UCAUCCAGCUGACUCGUUU 622 14091 oooooooooooosssssso Pm0fff0ff0000m00m00 AGAUUCAUCAGAAUGGUGA 623 14092 oooooooooooosssssso Pm00ffff00fmm0m000m0 UGACCUCAGUCCAUAAACC 624 14093 oooooooooooosssssso Pm0f00f0000mmm0mm000 AAUGGUGAGACUCAUCAGA 625 14094 oooooooooooosssssso Pmff00fffff00mmm0m000 UUUGACCUCAGUCCAUAAA 626 14095 oooooooooooosssssso Pmff0f00ff0m0000mmm0 UUCAUGGCUGUGAAAUUCA 627 14096 oooooooooooosssssso Pm00f00f0000mmm0mm00 GAAUGGUGAGACUCAUCAG 628 14097 oooooooooooosssssso Pm00ffffff0mmm0m0m00 UGGCUUUCCGCUUAUAUAA 629 14098 oooooooooooosssssso Pmf00ffffff0mmm0m0m0 UUGGCUUUCCGCUUAUAUA 630 14099 oooooooooooosssssso Pmf0fff0f0f00mm0m000 UCAUCCAUGUGGUCAUGGC 631 14100 oooooooooooosssssso Pmf0f00ff0f00mmmmm00 AUGUGGUCAUGGCUUUCGU 632 14101 oooooooooooosssssso Pmf00ff0f00mmmmm0mm0 GUGGUCAUGGCUUUCGUUG 633 14102 oooooooooooosssssso Pmff00fffffmmmm0m00 AUUGGCUUUCCGCUUAUAU 634 14103 oooooooooooosssssso Pm00f0f0000mmmm000m0 AAAUACGAAAUUUCAGGUG 635 14104 oooooooooooosssssso Pm000f0f0000mmmm000 AGAAAUACGAAAUUUCAGG 636 14105 oooooooooooosssssso Pm00ff0f00fmmmm0mm00 UGGUCAUGGCUUUCGUUGG 637 14106 oooooooooooosssssso Pmf0ff0fff0m0m00mm00 AUAUCAUCCAUGUGGUCAU 638 14107 oooooooooooosssssso Pm0f0f0000fmmm000m00 AAUACGAAAUUUCAGGUGU 639 14108 oooooooooooosssssso Pm0ff000000mm0mmm00 AAUCAGAAGGCGCGUUCAG 640 10109 oooooooooooosssssso Pmfff0f000000m0m0000 AUUCAUGAGAAAUACGAAA 641 14110 oooooooooooosssssso Pmf0fff0f0000000m000 CUAUUCAUGAGAGAAUAAC 642 14111 oooooooooooosssssso Pmfff0ff000mmm0mmm00 UUUCGUUGGACUUACUUGG 643 14112 oooooooooooosssssso Pmf0fffff0fm0mm00mm0 UUGCUCUCAUCAUUGGCUU 644 14113 oooooooooooosssssso Pmff00fffffmmmmmmm0 UUCAACUCCUCGCUUUCCA 645 14114 oooooooooooosssssso Pm00ff0ff00mm0m0mm00 UGACUAUCAAUCACAUCGG 646 14115 oooooooooooosssssso Pm0f0f0ff0mmm00mmm0 AGAUGCACUAUCUAAUUCA 647 14116 oooooooooooosssssso Pm0f000f0f0m0mmm00m0 AAUAGAUACACAUUCAACC 648 14117 oooooooooooosssssso Pmffffff0f0000m000m0 UUCUUCUAUAGAAUGAACA 649 14118 oooooooooooosssssso Pm0ff0ff000m00mm0m00 AAUUGCUGGACAACCGUGG 650 14119 oooooooooooosssssso Pmf0ffffff0m0m0m0000 UCGCUUUCCAUGUGUGAGG 651 14120 oooooooooooosssssso Pm00fff000fm0mmm0m00 UAAUCUGGACUGCUUGUGG 652 14121 oooooooooooosssssso Pmf0f0fff00mm00m0000 ACACAUUCAACCAAUAAAC 653 14122 oooooooooooosssssso Pmfff0ffff0m00mm0mm0 ACUCGUUUCAUAACUGUCC 654 14123 oooooooooooosssssso Pmf00fff000mm0mmm0m0 AUAAUCUGGACUGCUUGUG 655 14124 oooooooooooosssssso Pmffff0fff0m0m00mmm0 UUUCCGCUUAUAUAAUCUG 656 14125 oooooooooooosssssso Pm0fff00ff00m0m00m00 UGUUUAACUGGUAUGGCAC 657 14126 oooooooooooosssssso Pm0f0000f000m0m000m0 UAUAGAAUGAACAUAGACA 658 14127 oooooooooooosssssso Pmffffff00fm0m0mmm0 UUUCCUUGGUCGGCGUUUG 659 14128 oooooooooooosssssso Pmf0f0f0ff0mmm00mmm0 GUAUGCACCAUUCAACUCC 660 14129 oooooooooooosssssso Pmf00ff0ff0m0m0m0mm0 UCGGCCAUCAUAUGUGUCU 661 14130 oooooooooooosssssso Pm0fff000ff0mmm0m000 AAUCUGGACUGCUUGUGGC 662 14132 oooooooooooosssssso Pmf0ff0000f0mmm0mm00 ACAUCGGAAUGCUCAUUGC 663 14133 oooooooooooosssssso Pm00fffff00mm0mm00m0 AAGUUCCUGACUAUCAAUC 664 14134 oooooooooooosssssso Pmf00ff000f0m0000m00 UUGACUAAAUGCAAAGUGA 665 14135 oooooooooooosssssso Pm0fff0ff000mm00m00 AGACUCAUCAGACUGGUGA 666 14136 oooooooooooosssssso Pmf0f0f0f0fmm0mm0m00 UCAUAUGUGUCUACUGUGG 667 14137 oooooooooooosssssso Pmf0fffff0fmm0m00m00 AUGUCCUCGUCUGUAGCAU 668 14138 oooooooooooosssssso Pm00fff0f00mm00mmmm0 GAAUUCACGGCUGACUUUG 669 14139 oooooooooooosssssso Pmf0fffff000mmm000m0 UUAUUUCCAGACUCAAAUA 670 14140 oooooooooooosssssso Pm000ff0f000mm000mm0 GAAGCCACAAACUAAACUA 671 14141 oooooooooooosssssso Pmffff0ff000mmm0mmm0 CUUUCGUUGGACUUACUUG 672 14142 oooooooooooosssssso Pmfff0f0000mmmmmm000 GUCUGCGAAACUUCUUAGA 673 14143 oooooooooooosssssso Pm0f0fff0ff0mmmmm0m0 AAUGCUCAUUGCUCUCAUC 674 14144 oooooooooooosssssso Pmf0f0ff0ffm00mmm0m0 AUGCACUAUCUAAUUCAUG 675 14145 oooooooooooosssssso Pmff0f0f0f0mm0mmm000 CUUGUAUGCACCAUUCAAC 676 14146 oooooooooooosssssso Pm00fff0fffm0m00mm00 UGACUCGUUUCAUAACUGU 677 14147 oooooooooooosssssso Pmff00f0fffm00mm0mm0 UUCAGCACUCUGGUCAUCC 678 14118 oooooooooooosssssso Pm00fff0f00mm0m00000 AAAUUCAUGGCUGUGGAAU 679 14149 oooooooooooosssssso Pmf0fff00ff00m000mm0 ACAUUCAACCAAUAAACUG 680 14150 oooooooooooosssssso Pm0f0f0fff00mm00m000 UACACAUUCAACCAAUAAA 681 14151 oooooooooooosssssso Pmff00ff0ffmmm000mm0 AUUAGUUAUUUCCAGACUC 682 14152 oooooooooooosssssso Pmffff0fff0m00000000 UUUCUAUUCAUGAGAGAAU 683 14153 oooooooooooosssssso Pmff00ff0ff00m000mm0 UUCGGUUGCUGGCAGGUCC 684 14154 oooooooooooosssssso Pm0f0f0f0000m00m0mm0 CAUGUGUGAGGUGAUGUCC 685 14155 oooooooooooosssssso Pmf0ff0fff00mmmmmm00 GCACCAUUCAACUCCUCGC 686 14156 oooooooooooosssssso Pm0fff00ff00mmm0mmm0 CAUCCAGCUGACUCGUUUC 687 14157 oooooooooooosssssso Pmfffff0fff0m0m00mm0 CUUUCCGCUUAUAUAAUCU 688 14158 oooooooooooosssssso Pm0ff0f0ff0000m0mmm0 AAUCACAUCGGAAUGCUCA 689 14159 oooooooooooosssssso Pmf0f0ff00fm0mmmmm00 ACACAUUAGUUAUUUCCAG 690 14160 oooooooooooosssssso Pmfff0f0000m000m0m00 UUCUAUAGAAUGAACAUAG 691 14161 oooooooooooosssssso Pm0f00f00f00mmm0m0m0 UACAGUGAUAGUUUGCAUU 692 14162 oooooooooooosssssso Pmf000f00ff00m0mm0m0 AUAAGCAAUUGACACCACC 693 14163 oooooooooooosssssso Pmff0ff00ff0mm000m00 UUUAUUAAUUGCUGGACAA 694 14164 oooooooooooosssssso Pmf0ff0000fmmmm0000 UCAUCAGAGUCGUUCGAGU 695 14165 oooooooooooosssssso Pmf000ff0f0mm0mm0mm0 AUAAACCACACUAUCACCU 696 14166 oooooooooooosssssso Pmf0ff0ff00mmmmmm0m0 UCAUCAUUGGCUUUCCGCU 697 14167 oooooooooooosssssso Pmfffff00fm0mm00mm0 AGUUCCUGACUAUCAAUCA 698 14168 oooooooooooosssssso Pmff0f00ff00mmmm0000 UUCACGGCUGACUUUGGAA 699 14169 oooooooooooosssssso Pmffff0f00f00m000mm0 UUCUCAUGGUAGUGAGUUU 700 14170 oooooooooooosssssso Pm0ff00fff0mmm00mm00 AAUCAGCCUGUUUAACUGG 701 14171 oooooooooooosssssso Pm0ffff00f0mmmm00mm0 GGUUUCAGCACUCUGGUCA 702 14172 oooooooooooosssssso Pmff0000f0fmm0mm0mm0 AUCGGAAUGCUCAUUGCUC 703 17173 oooooooooooosssssso Pm00fF0f0000mmm0m000 UGGCUGUGGAAUUCACGGC 704 14174 oooooooooooosssssso Pm000f00ff00m0mm0mm0 UAAGCAAUUGACACCACCA 705 14175 oooooooooooosssssso Pm00fffff0f00m00m000 CAAUUCUCAUGGUAGUGAG 706 14176 oooooooooooosssssso Pm00fffff0fm000mmm00 UGGCUUUCGUUGGACUUAC 707 14177 oooooooooooosssssso Pm0ff00f00fm00mmm0m0 AAUCAGUGACCAGUUCAUC 708 14178 oooooooooooosssssso Pmfff0f000mm0m0mm00 AGUCCAUAAACCACACUAU 709 14179 oooooooooooosssssso Pm00f0ffff00mm0mmm00 CAGCACUCUGGUCAUCCAG 710 14180 oooooooooooosssssso Pm0ff00ff0f0mm0000m0 UAUCAAUCACAUCGGAAUG 711 14181 oooooooooooosssssso Pmfff0f00ff00mmmm000 AUUCACGGCUGACUUUGGA 712 14182 oooooooooooosssssso Pmf000f0f0f0mmm00mm0 AUAGAUACACAUUCAACCA 713 14183 oooooooooooosssssso Pmffff000ffm000m0000 UUUCCAGACUCAAAUAGAU 714 14184 oooooooooooosssssso Pmf00ff0ff000m00mm00 UUAAUUGCUGGACAACCGU 715 14185 oooooooooooosssssso Pm0ff00ff0fm000m00m0 UAUUAAUUGCUGGACAACC 716 14186 oooooooooooosssssso Pmff0fff000mm00m000 AGUCGUUCGAGUCAAUGGA 717 14187 oooooooooooosssssso Pmff0ff00f000mmm0m00 GUUGCUGGCAGGUCCGUGG 718

TABLE 3 OHang Oligo Sense SEQ ID Number Number Chem. Sense Backbone Sense Chemistry Sense Sequence ID NO: APOB- 12138 ch1 ooooooooooooooo 000000000000000000 GUCAUCACACUGAAUACCAAU 176 10167-20-12138 ooooso 00 APOB- 121389 chl ooooooooooooooo 000000000000000000 GUGAUCAGACUCAAUACGAAU 177 10167-20-12139 ooooso 00 MAP4K4- 12266 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 178 2931-13-12266 MAP4K4- 12293 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 179 2931-13-12293 MAP4K4- 12383 chl ooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 180 2931-16-12383 MAP4K4- 12384 chl ooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 181 2931-16-12384 MAP4K4- 12385 chl ooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 182 2931-16-12385 MAP4K4- 12386 chl oooooooooosso 0mm0m00000mmm0 CUGUGGAAGUCUA 183 2931-16-12386 MAP4K4- 12387 chl ooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 184 2931-16-12387 MAP4K4- 12388 chl ooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 185 2931-16-12388 MAP4K4- 12432 chl ooooooooooooo DY547mm0m00000mmm0 CUGUGGAAGUCUA 186 2931-13-12432 MAP4K4- 12266.2 chl oooooooooooss mm0m00000mmm0 CUGUGGAAGUCUA 187 2931-13-12266.2 APOB-- 12434 chl ooooooooooooooo 000000000000000000 GUCAUCACACUGAAUACCAAU 188 21-12434 ooooso 00 APOB-- 12435 chl ooooooooooooooo DY5470000000000000 GUGAUCAGACUCAAUACGAAU 189 21-12435 ooooso 0000000 MAP4K4- 12451 chl oooooooooooss 0mm0m00000mmm0 CUGUGGAAGUCUA 190 2931-16-12451 MAP4K4- 12452 chl oooooooooooss mm0m00000mmm0 CUGUGGAAGUCUA 191 2931-16-12452 MAP4K4- 12453 chl oooooooooooss mm0m00000mmm0 CUGUGGAAGUCUA 192 2931-16-12453 MAP4K4- 12454 chl oooooooooooss 0mm0m00000mmm0 CUGUGGAAGUCUA 193 2931-17-12454 MAP4K4- 12455 chl oooooooooooss mm0m00000mmm0 CUGUGGAAGUCUA 194 2931-17-12455 MAP4K4- 12456 chl oooooooooooss mm0m00000mmm0 CUGUGGAAGUCUA 195 2931-19-12456 --27-12480 12480 chl ooooooooooooooo DY547mm0f000f0055f UCAUAGGUAACCUCUGGUUGA 196 ooooooooosso 5f00mm00000m000 AAGUGA --27-12481 12481 chl ooooooooooooooo DY547mm05f05000f05 CGGCUACAGGUGCUUAUGAAG 197 ooooooooosso ff0m00000000m00 AAAGUA APOB- 12505 chl ooooooooooooooo 000000000000000000 GUCAUCACACUGAAUACCAAU 198 10167-21-12505 ooooos 000 APOB- 12506 chl ooooooooooooooo 000000000000000000 GUGAUCAGACUCAAUACGAAU 199 10167-21-12506 ooooos 000 MAP4K4- 12539 chl oooooooooooss DY547mm0m00000mmm0 CUGUGGAAGUCUA 200 2931-16-12539 APOB- 12505.2 chl ooooooooooooooo 000000000000000000 GUCAUCACACUGAAUACCAAU 201 10167-21-12505.2 ooooso 00 APOB- 12506.2 chl ooooooooooooooo 000000000000000000 GUGAUCAGACUCAAUACGAAU 202 10167-21-12506.2 ooooso 00 MAP4K4-- 12565 Chl ooooooooooooo m0m0000m0mmm0 UGUAGGAUGUCUA 203 13-12565 MAP4K4- 12386.2 chl ooooooooooooo 0mm0m00000mmm0 CUGUGGAAGUCUA 204 2931-16-12386.2 MAP4K4- 12815 chl ooooooooooooo m0m0m0m0mk0m0m0m0m CUGUGGAAGUCUA 205 2931-13-12815 0m0m0m0m0 APOB-- 12957 Chl oooooooooooss 0mmmmmmmmmmmmm ACUGAAUACCAAU 206 13-12957 TEG MAP4K4-- 12983 chl oooooooooooss mm0m00000mmm0 CUGUGGAAGUCUA 207 16-12983 MAP4K4-- 12984 Chl oooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 208 16-12984 MAP4K4-- 12985 chl oooooooooosso mmmmmmmmmmmmm CUGUGGAAGUCUA 209 16-12985 MAP4K4-- 12986 chl oooooooooosso mmmmmmmmmmmmm CUGUGGAAGUCUA 210 16-12986 MAP4K4-- 12987 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 211 16-12987 MAP4K4-- 12988 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 212 16-12988 MAP4K4-- 12989 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 213 16-12989 MAP4K4-- 12990 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 214 16-12990 MAP4K4-- 12991 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 215 16-12991 MAP4K4-- 12992 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 216 16-12992 MAP4K4-- 12993 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 217 16-12993 MAP4K4-- 12994 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 218 16-12994 MAP4K4-- 12995 chl oooooooooosso mm0m00000mmm0 CUGUGGAAGUCUA 219 16-12995 MAP4K4- 13012 chl ooooooooooooooo 000000000000000000 AGAGUUCUGUGGAAGUCUA 220 2931-19-13012 oooo 000 MAP4K4- 13016 chl ooooooooooooooo DY5470000000000000 AGAGUUCUGUGGAAGUCUA 221 2931-19-13016 oooo 00000000 PPIB-- 13021 Chl ooooooooooooo 0mmm00mm0m000 AUUUGGCUACAAA 222 13-13021 pGL3- 13038 chl ooooooooooooo 00m000m0m00mmm ACAAAUACGAUUU 223 1172-13-13038 pGL3- 13040 chl ooooooooooooo DY5470m000m0m00mmm ACAAAUACGAUUU 224 1172-13-13040 --16-13047 13047 Chl oooooooooooooo mm0m00000mmm0 CUGUGGAAGUCUA 225 SOD1- 13090 chl ooooooooooooo 00m00000000m0 AAUGAAGAAAGUA 226 530-13-13090 SOD1- 13091 chl ooooooooooooo 000m00000m000 AGGUGGAAAUGAA 227 523-13-13091 SOD1- 13092 chl ooooooooooooo 000000m0m0000 AGAAAGUACAAAG 228 535-13-13092 SOD1- 13093 chl ooooooooooooo 00000m0m00000 GAAAGUACAAAGA 229 536-13-13093 SOD1- 13094 chl ooooooooooooo 0m0m00mm0mm00 AUGUGACUGCUGA 230 596-13-13094 SOD1- 13095 chl ooooooooooooo 000mmm000m00m AGACUUGGGCAAU 231 385-13-13095 SOD1- 13096 chl ooooooooooooo 0mmmm000m0000 AUUUCGAGCAGAA 232 195-13-13096 APOB- 13115 Chl ooooooooooooo 0mmm0000000m0 AUCUGGAGAAACA 233 4314-13-13115 APOB- 13116 Chl ooooooooooooo mm0000m000000 UCAGAACAAGAAA 234 3384-13-13116 APOB- 13117 Chl ooooooooooooo 00mmm0mmm0mm0 GACUCAUCUGCUA 235 3547-13-13117 APOB- 13118 Chl ooooooooooooo 0000000m00m0m GGAGAAACAACAU 236 4318-13-13118 APOB- 13119 Chl ooooooooooooo 00mmmmmm000m0 AGUCCCUCAAACA 237 3714-13-13119 PPIB-- 13136 Chl oooooooooooooo 00mm0m00000m0 GGCUACAAAAACA 238 16-13136 APOB- 13154 chl oooooooooooooo 000mmm0000000m0 AGAUCUGGAGAAACA 239 4314-15-13154 APOB- 13155 chl oooooooooooooo m000mmm0mmm0mm0 UGGACUCAUCUGCUA 240 3547-15-13155 APOB- 13157 chl oooooooooooooo mm0000000m00m0m CUGGAGAAACAACAU 241 4318-15-13157 APOB- 13158 chl oooooooooooooo 000mmmmmm000m0 AGAGUCCCUCAAACA 242 3714-15-13158 AP0B-- 13159 chl oooooooooooo 0mm000m0mm00m ACUGAAUACCAAU 243 13-13159 APOB-- 13160 chl oooooooooooooo 0m0mm000m0mm00m ACACUGAAUACCAAU 244 15-13160 SOD1- 13163 chl ooooooooooooo 00m00000000m0 AAUGAAGAAAGUA 245 530-16-13163 SOD1- 13164 chl ooooooooooooo 000m00000m000 AGGUGGAAAUGAA 246 523-16-13164 SOD1- 13165 chl ooooooooooooo 000000m0m0000 AGAAAGUACAAAG 247 535-16-13165 SOD1- 13166 chl ooooooooooooo 00000m0m00000 GAAAGUACAAAGA 248 536-16-13166 SOD1- 13167 chl ooooooooooooo 0m0m00mm0mm00 AUGUGACUGCUGA 249 396-16-13167 SOD1- 13168 chl ooooooooooooo 000mmm000m00m AGACUUGGGCAAU 250 385-16-13168 SOD1- 13169 chl ooooooooooooo 0mmmm000m0000 AUUUCGAGCAGAA 251 195-16-13169 pGL3- 13170 chl ooooooooooooo 0m000m0m00mmm ACAAAUACGAUUU 252 1172-16-13170 pGL3- 13171 chl ooooooooooooo DY5470m000m0m00mmm ACAAAUACGAUUU 253 1172-16-13171 MAP4k4- 13189 chl ooooooooooooooo 000000000000000000 AGAGUUCUGUGGAAGUCUA 254 2931-19-13189 oooo 000 CTGF- 13190 Chl ooooooooooooo 0m0000000m0m0 ACAGGAAGAUGUA 255 1222-13-13190 CTGF- 13192 Chl ooooooooooooo 000m0000m0mmm GAGUGGAGCGCCU 256 813-13-13192 CTGF- 13194 Chl ooooooooooooo m00mm000000m0 CGACUGGAAGACA 257 747-13-13194 CTGF- 13196 Chl ooooooooooooo 0000m0mmm0mmm GGAGCGCCUGUUC 258 817-13-13196 CTGF- 13198 Chl ooooooooooooo 0mm0mm0m00mm0 GCCAUUACAACUG 259 1174-13-13198 CTGF- 13200 Chl ooooooooooooo 000mmmmmm00mm GAGCUUUCUGGCU 260 1005-13-13200 CTGF- 13202 Chl ooooooooooooo 00m0000m0mmm0 AGUGGAGCGCCUG 261 814-13-13202 CTGF- 13204 Chl ooooooooooooo m0000m0mmm0mm UGGAGCGCCUGUU 262 816-13-13204 CTGF- 13206 Chl ooooooooooooo 0mmm000mmmmmm GUUUGAGCUUUCU 263 1001-13-13206 CTGF- 13208 Chl ooooooooooooo m0mm0mm0m00mm UGCCAUUACAACU 264 1173-13-13208 CTGF- 13210 Chl ooooooooooooo 0mm000000m0m0 ACUGGAAGACACG 265 749-13-13210 CTGF- 13212 Chl ooooooooooooo 00mm0mmm00mmm AACUGCCUGGUCC 266 792-13-13212 CTGF- 13214 Chl ooooooooooooo 000mmm0m0mmm0 AGACCUGUGCCUG 267 1162-13-13214 CTGF- 13216 Chl ooooooooooooo m0000m0000m0m CAGAGUGGAGCGC 268 811-13-13216 CTGF- 13218 Chl ooooooooooooo mmm00mmm000mm CCUGGUCCAGACC 269 797-13-13218 CTGF- 13220 Chl ooooooooooooo mm0mm0m00mm0m CCAUUACAACUGU 270 1175-13-13220 CTGF- 13222 Chl ooooooooooooo mm0mm0mm0m00m CUGCCAUUACAAC 271 1172-13-13222 CTGF- 13224 Chl ooooooooooooo 0mm0m00mm0mmmm AUUACAACUGUCC 272 1177-13-13224 CTGF- 13226 Chl ooooooooooooo m0mm0m00mm0mm CAUUACAACUGUC 273 1176-13-13226 CTGF- 13228 Chl ooooooooooooo 0000m0000m0mm AGAGUGGAGCGCC 274 812-13-13228 CTGF- 13230 Chl ooooooooooooo 0mm00mm000000 ACCGACUGGAAGA 275 745-13-13230 CTGF- 13232 Chl ooooooooooooo 0m0m0m00000m0 AUGUACGGAGACA 276 1230-13-13232 CTGF- 13234 Chl ooooooooooooo 0mmmm0m0000mm GCCUUGCGAAGCU 277 920-13-13234 CTGF- 13238 Chl ooooooooooooo 0mm0m000000m0 GCUGCGAGGAGUG 278 679-13-13238 CTGF- 13238 Chl ooooooooooooo 0mmm0mm000mmm GCCUAUCAAGUUU 279 992-13-13238 CTGF- 13240 Chl ooooooooooooo 00mmmm0m0000m AAUUCUGUGGAGU 280 1045-13-13240 CTGF- 13242 Chl ooooooooooooo m0m0m00000m0m UGUACGGAGACAU 281 1231-13-13242 CTGF- 13244 Chl ooooooooooooo 00mmm0mm000mm AGCCUAUCAAGUU 282 991-13-13244 CTGF- 13246 Chl ooooooooooooo m000mmm000mmm CAAGUUUGAGCUU 283 998-13-13246 CTGF- 13248 Chl ooooooooooooo mm0m0000m0m0m CUGUGGAGUAUGU 284 1049-13-13248 CTGF- 13250 Chl ooooooooooooo 000mmmm0m0000 AAAUUCUGUGGAG 285 1044-13-13250 CTGF- 13252 Chl ooooooooooooo mmmm00m00m0m0 UUUCAGUAGCACA 286 1327-13-13252 CTGF- 13254 Chl ooooooooooooo m00m00m0mmmmm CAAUGACAUCUUU 287 1196-13-13254 CTGF- 13256 Chl ooooooooooooo 00m0mm00m0m0m AGUACCAGUGCAC 288 562-13-13256 CTGF- 13258 Chl ooooooooooooo 000000m0m0mmm GGAAGACACGUUU 289 752-13-13258 CTGF- 13260 Chl ooooooooooooo mm0mm000mmm00 CUAUCAAGUUUGA 290 944-13-13260 CTGF- 13262 Chl ooooooooooooo 00mm000mmmm0m AGCUAAAUUCUGU 291 1040-13-13262 CTGF- 13264 Chl ooooooooooooo 000m0000m0m00 AGGUAGAAUGUAA 292 1984-13-13264 CTGF- 13266 Chl ooooooooooooo 00mm00mm00mmm AGCUGAUCAGUUU 293 2043-13-13266 CTGF- 13268 Chl ooooooooooooo mmmm0mmm000m0 UUCUGCUCAGAUA 294 2043-13-13268 CTGF- 13270 Chl ooooooooooooo mm0mmm000mm00 UUAUCUAAGUUAA 295 1892-13-13270 CTGF- 13272 Chl ooooooooooooo m0m0m000m00m0 UAUACGAGUAAUA 296 1567-13-13272 CTGF- 13274 Chl ooooooooooooo 00mm000m00mmm GACUGGACAGCUU 297 1780-13-13274 CTGF- 13276 Chl ooooooooooooo 0m00mmmmm0mm0 AUGGCCUUUAUUA 298 2162-13-13276 CTGF- 13278 Chl ooooooooooooo 0m0mm000mm000 AUACCGAGCUAAA 299 1034-13-13278 CTGF- 13280 Chl ooooooooooooo mm0mm00000m0m UUGUUGAGAGUGU 300 2264-13-13280 CTGF- 13282 Chl ooooooooooooo 0m0m0mm000mm0 ACAUACCGAGCUA 301 1032-13-13282 CTGF- 13284 Chl ooooooooooooo 00m0000000mm0 AGCAGAAAGGUUA 302 1535-13-13284 CTGF- 13286 Chl ooooooooooooo 00mm0mmmmmm00 AGUUGUUCCUUAA 303 1694-13-13286 CTGF- 13288 Chl ooooooooooooo 0mmm0000m0m00 AUUUGAAGUGUAA 304 1588-13-13288 CTGF- 13290 Chl ooooooooooooo 000mm00mmm000 AAGCUGACCUGGA 305 928-13-13290 CTGF- 13292 Chl ooooooooooooo 00mm0m0000000 GGUCAUGAAGAAG 306 1133-13-13292 CTGF- 13294 Chl ooooooooooooo 0m00mm000mmmm AUGGUCAGGCCUU 307 912-13-13294 CTGF- 13296 Chl ooooooooooooo 00000m0m0mmm0 GAAGACACGUUUG 308 753-13-13296 CTGF- 13298 Chl ooooooooooooo 000mmmm0m0000 AGGCCUUGCGAAG 309 918-13-13298 CTGF- 13300 Chl ooooooooooooo m0mm0mm00000 UACCGACUGGAAG 310 744-13-13300 CTGF- 13302 Chl ooooooooooooo 0mm0m0000mm0 ACCGCAAGAUCGG 311 466-13-13302 CTGF- 13304 Chl ooooooooooooo m000mmmm0m000 CAGGCCUUGCGAA 312 917-13-13304 CTGF- 13306 Chl ooooooooooooo m000mm000mmmm CGAGCUAAAUUCU 313 1038-13-13306 CTGF- 13308 Chl ooooooooooooo mmm0m0000m0m0 UCUGUGGAGUAUG 314 1048-13-13308 CTGF- 13310 Chl ooooooooooooo m00000m0m00m0 CGGAGACAUGGCA 315 1235-13-13310 CTGF- 13312 Chl ooooooooooooo 0m00m00m0mmmm AUGACAACGCCUC 316 868-13-13312 CTGF- 13314 Chl ooooooooooooo 0000mm0m00000 GAGGUCAUGAAGA 317 1131-13-13314 CTGF- 13316 Chl ooooooooooooo m000mmmm0m000 UAAAUUCUGUGGA 318 1043-13-13316 CTGF- 13318 Chl ooooooooooooo m000000m0m0mm UGGAAGACACGUU 319 751-13-13318 CTGF- 13320 Chl ooooooooooooo 0000m0m0m0000 AAGAUGUACGGAG 320 1227-13-13320 CTGF- 13322 Chl ooooooooooooo 00m00m00m0mmm AAUGACAACGCCU 321 867-13-13322 CTGF- 13324 Chl ooooooooooooo 00m0000mm0m00 GGCGAGGUCAUGA 322 1128-13-13324 CTGF- 13326 Chl ooooooooooooo 00m0m0mmm00mm GACACGUUUGGCC 323 756-13-13326 CTGF- 13328 Chl ooooooooooooo 0m00000m0m00m ACGGAGACAUGGC 324 1234-13-13328 CTGF- 13330 Chl ooooooooooooo mm000mmmm0m00 UCAGGCCUUGCGA 325 916-13-13330 CTGF- 13332 Chl ooooooooooooo 0m0000mm00mmm GCGAAGCUGACCU 326 925-13-13332 CTGF- 13334 Chl ooooooooooooo 000000m0m0m00 GUGACUUCGGCUC 328 1225-13-13334 CTGF- 13336 Chl ooooooooooooo 0m00mmmm00mmm GUGACUUCGGCUC 328 445-13-13336 CTGF- 13338 Chl ooooooooooooo m00mmmm00mmmm UGACUUCGGCUCC 329 446-13-13338 CTGF- 13340 Chl ooooooooooooo m00mm000mmmm0 UGGUCAGGCCUUG 330 913-13-13340 CTGF- 13342 Chl ooooooooooooo mm000mmm000mm UCAAGUUUGAGCU 331 997-13-13342 CTGF- 13344 Chl ooooooooooooo 0mm0000mm0m00 GCCAGAACUGCAG 332 277-13-13344 CTGF- 13346 Chl ooooooooooooo m0000m0m0m0mm UGGAGUAUGUACC 333 1052-13-13346 CTGF- 13348 Chl ooooooooooooo 0mm0000000m00 GCUAGAGAAGCAG 334 887-13-13348 CTGF- 13350 Chl ooooooooooooo 00mm000mmmm0m GGUCAGGCCUUGC 335 914-13-13350 CTGF- 13352 Chl ooooooooooooo 000mm000mmmm0 GAGCUAAAUUCUG 336 1039-13-13352 CTGF- 13354 Chl ooooooooooooo 0000m0m0mmm00 AAGACACGUUUGG 337 754-13-13354 CTGF- 13356 Chl ooooooooooooo m0000mm0m0000 CGAGGUCAUGAAG 338 1130-13-13354 CTGF- 13358 Chl ooooooooooooo 00mmmm0m0000m GGCCUUGCGAAGC 339 919-13-13358 CTGF- 13360 Chl ooooooooooooo mmm0m0000mm00 CUUGCGAAGCUGA 340 922-13-13360 CTGF- 13362 Chl ooooooooooooo mm00mm000000m CCGACUGGAAGAC 341 746-13-13362 CTGF- 13364 Chl ooooooooooooo mmm0mm000mmm0 CCUAUCAAGUUUG 342 993-13-13364 CTGF- 13366 Chl ooooooooooooo m0mmmm0000mmm UGUUCCAAGACCU 343 825-13-13366 CTGF- 13368 Chl ooooooooooooo m0000mm00mmm0 CGAAGCUGACCUG 344 926-13-13368 CTGF- 13370 Chl ooooooooooooo mm0m0000mm00m UUGCGAAGCUGAC 345 923-13-13370 CTGF- 13372 Chl ooooooooooooo m00m00m00m0mm CAAUGACAACGCC 346 866-13-13372 CTGF- 13374 Chl ooooooooooooo 0m0mm00m0m0m0 GUACCAGUGCACG 347 563-13-13374 CTGF- 13376 Chl ooooooooooooo mmm0mmmm0000m CCUGUUCCAAGAC 348 823-13-13376 CTGF- 13378 Chl ooooooooooooo m0m00000m0m00 UACGGAGACAUGG 349 1233-13-13378 CTGF- 13380 Chl ooooooooooooo m0m0000mm00mm UGCGAAGCUGACC 350 924-13-13380 CTGF- 13382 Chl ooooooooooooo mmmm0m0000mm0 CCUUGCGAAGCUG 351 921-13-13382 CTGF- 13384 Chl ooooooooooooo mm0m00mmmm00m CUGUGACUUCGGC 352 443-13-13384 CTGF- 13386 Chl ooooooooooooo 0mm000mmmm0m0 GCUAAAUUCUGUG 353 1041-13-13386 CTGF- 13388 Chl ooooooooooooo mm000mmmm0m00 CUAAAUUCUGUGG 354 1042-13-13388 CTGF- 13390 Chl ooooooooooooo 000m0m0mmm00m AGACACGUUUGGC 355 755-13-13390 CTGF- 13392 Chl ooooooooooooo mm0m0000mm00m CCGCAAGAUCGGC 356 467-13-13392 CTGF- 13394 Chl ooooooooooooo m0mm000mmm000 UAUCAAGUUUGAG 357 995-13-13394 CTGF- 13396 Chl ooooooooooooo 0000mm00mmm00 GAAGCUGACCUGG 358 927-13-13396 SPP1- 13398 Chl ooooooooooooo mmm0m000mm000 CUCAUGAAUUAGA 359 1025-13-13398 SPP1- 13400 Chl ooooooooooooo mm0000mm00mm0 CUGAGGUCAAUUA 360 1049-13-13400 SPP1- 13402 Chl ooooooooooooo 0000mm00mm000 GAGGUCAAUUAAA 361 1051-13-13402 SPP1- 13404 Chl ooooooooooooo mmm0000mm00mm UCUGAGGUCAAUU 362 1048-13-13404 SPP1- 13406 Chl ooooooooooooo m0000mm00mm00 UGAGGUCAAUUAA 363 1050-13-13406 SPP1- 13408 Chl ooooooooooooo mmmm0000mm00m UUCUGAGGUCAAU 364 1047-13-13408 SPP1- 13410 Chl ooooooooooooo 0mm00mm000m00 GUCAGCUGGAUGA 365 800-13-13410 SPP1- 13412 Chl ooooooooooooo mmmm00m000mmm UUCUGAUGAAUCU 366 492-13-13412 SPP1- 13414 Chl ooooooooooooo m000mm0000mm0 UGGACUGAGGUCA 367 612-13-13414 SPP1- 13416 Chl ooooooooooooo 000mmmm0mm0mm GAGUCUCACCAUU 368 481-13-13416 SPP1- 13418 Chl ooooooooooooo 00mm0000mm000 GACUGAGGUCAAA 369 614-13-13418 SPP1- 13420 Chl ooooooooooooo mm0m00mm0m000 UCACAGCCAUGAA 370 951-13-13420 SPP1- 13422 Chl ooooooooooooo 00mmmm0mm0mmm AGUCUCACCAUUC 371 482-13-13422 SPP1- 13424 Chl ooooooooooooo 000m000000mm0 AAGCGGAAAGCCA 372 856-13-13424 SPP1- 13426 Chl ooooooooooooo 00m000000mm00 AGCGGAAAGCCAA 373 857-13-13426 SPP1- 13428 Chl ooooooooooooo 0mm0m0m000m00 ACCACAUGGAUGA 374 365-13-13428 SPP1- 13430 Chl ooooooooooooo 0mm0m00mm0m0m GCCAUGACCACAU 375 359-13-13430 SPP1- 13432 Chl ooooooooooooo 000mm0m00mm0m AAGCCAUGACCAC 376 357-13-13432 SPP1- 13434 Chl ooooooooooooo 0m000000mm00m GCGGAAAGCCAAU 377 858-13-13434 SPP1- 13436 Chl ooooooooooooo 000mmmm0m0mmm AAAUUUCGUAUUU 378 1012-13-13436 SPP1- 13438 Chl ooooooooooooo 0mmmm0m0mmmmm AUUUCGUAUUUCU 379 1014-13-13438 SPP1- 13440 Chl ooooooooooooo 0000mm0m00mm0 AAAGCCAUGACCA 380 356-13-13440 SPP1- 13442 Chl ooooooooooooo 0m0m000m00m0m ACAUGGAUGAUAU 381 368-13-13442 SPP1- 13444 Chl ooooooooooooo 0000mmmm0m0mm GAAAUUUCGUAUU 382 1011-13-13444 SPP1- 13446 Chl ooooooooooooo 0m0mmmmmm00mm GCGCCUUCUGAUU 383 754-13-13446 SPP1- 13448 Chl ooooooooooooo 0mmmmmm0m000m AUUUCUCAUGAAU 384 1021-13-13448 SPP1- 13450 Chl ooooooooooooo mmmmm0m000m00 CUCUCAUGAAUAG 385 1330-13-13450 SPP1- 13452 Chl ooooooooooooo 000mmm00m0000 AAGUCCAACGAAA 386 346-13-13452 SPP1- 13454 Chl ooooooooooooo 0m00m00000m00 AUGAUGAGAGCAA 387 869-13-13454 SPP1- 13456 Chl ooooooooooooo 0m000000mm000 GCGAGGAGUUGAA 388 701-13-13456 SPP1- 13458 Chl ooooooooooooo m00mm00m00mm0 UGAUUGAUAGUCA 389 896-13-13458 SPP1- 13460 Chl ooooooooooooo 000m00m0m0mmm AGAUAGUGCAUCU 390 1035-13-13460 SPP1- 13462 Chl ooooooooooooo 0m0m0m0mmm0mm AUGUGUAUCUAUU 391 1170-13-13462 SPP1- 13464 Chl ooooooooooooo mmmm0m0000000 UUCUAUAGAAGAA 392 1282-13-13464 SPP1- 13466 Chl ooooooooooooo mm0mmm00m00mm UUGUCCAGCAAUU 393 1537-13-13466 SPP1- 13468 Chl ooooooooooooo 0m0m000000m00 ACAUGGAAAGCGA 394 692-13-13468 SPP1- 13470 Chl ooooooooooooo 0m00mmm000mm0 GCAGUCCAGAUUA 395 840-13-13470 SPP1- 13472 Chl ooooooooooooo m00mm000m0m0m UGGUUGAAUGUGU 396 1163-13-13472 SPP1- 13474 Chl ooooooooooooo mm0m0000m000m UUAUGAAACGAGU 397 789-13-13474 SPP1- 13476 Chl ooooooooooooo m00mmm000mm0m CAGUCCAGAUUAU 398 841-13-13476 SPP1- 13478 Chl ooooooooooooo 0m0m000m00000 AUAUAAGCGGAAA 399 852-13-13478 SPP1- 13480 Chl ooooooooooooo m0mm00mm000m0 UACCAGUUAAACA 400 209-13-13480 SPP1- 13482 Chl ooooooooooooo m0mmm0mmmm0m0 UGUUCAUUCUAUA 401 1276-13-13482 SPP1- 13484 Chl ooooooooooooo mm00mm0000000 CCGACCAAGGAAA 402 137-13-13484 SPP1- 13486 Chl ooooooooooooo 000m00m0m0m0m GAAUGGUGCAUAC 403 711-13-13486 SPP1- 13488 Chl ooooooooooooo 0m0m00m00mm00 AUAUGAUGGCCGA 404 582-13-13488 SPP1- 13490 Chl ooooooooooooo 00m00mmm000mm AGCAGUCCAGAUU 405 839-13-13490 SPP1- 13492 Chl ooooooooooooo 0m0mmm00mm000 GCAUUUAGUCAAA 406 1091-13-13492 SPP1- 13494 Chl ooooooooooooo 00m0mmmm00m0m AGCAUUCCGAUGU 407 884-13-13494 SPP1- 13496 Chl ooooooooooooo m00mm00000mmm UAGUCAGGAACUU 408 884-13-13496 SPP1- 13498 Chl ooooooooooooo m0m0mmm00mm00 UGCAUUUAGUCAA 409 1090-13-13498 SPP1- 13500 Chl ooooooooooooo 0mmm00m000mmm GUCUGAUGAGUCU 410 474-13-13500 SPP1- 13502 Chl ooooooooooooo m000m0m0m0m00 UAGACACAUAUGA 411 575-13-13502 SPP1- 13504 Chl ooooooooooooo m000m00000m0m CAGACGAGGACAU 412 671-13-13504 SPP1- 13506 Chl ooooooooooooo m00mm0m000mmm CAGCCGUGAAUUC 413 924-13-13506 SPP1- 13508 Chl ooooooooooooo 00mmm00000m00 AGUCUGGAAAUAA 414 1185-13-13508 SPP1- 13510 Chl ooooooooooooo 00mmm0m00mmmm AGUUUGUGGCUUC 415 1221-13-13510 SPP1- 13512 Chl ooooooooooooo 00mmm00m00000 AGUCCAACGAAAG 416 347-13-13512 SPP1- 13514 Chl ooooooooooooo 000mmmm0m000m AAGUUUCGCAGAC 417 634-13-13514 SPP1- 13516 Chl ooooooooooooo 00m00m000m0mm AGCAAUGAGCAUU 418 877-13-13516 SPP1- 13518 Chl ooooooooooooo mm000m00m0m0m UUAGAUAGUGCAU 419 1033-13-13518 SPP1- 13520 Chl ooooooooooooo m00m0m0m0m000 UGGUGCAUACAAG 420 714-13-13520 SPP1- 13522 Chl ooooooooooooo 0m0000m000mm0 AUGAAACGAGUCA 421 791-13-13522 SPP1- 13524 Chl ooooooooooooo mm0000m0mm000 CCAGAGUGCUGAA 422 813-13-13524 SPP1- 13526 Chl ooooooooooooo m00mm0m000mmm CAGCCAUGAAUUU 423 939-13-13526 SPP1- 13528 Chl ooooooooooooo 0mm00mm000m0m AUUGGUUGAAUGU 424 1161-13-13528 SPP1- 13530 Chl ooooooooooooo 00mm000m0m0m0 GGUUGAAUGUGUA 425 1164-13-13530 SPP1- 13532 Chl ooooooooooooo 00000m00mm00m GGAAAUAACUAAU 426 1190-13-13532 SPP1- 13534 Chl ooooooooooooo mm0m000m00000 UCAUGAAUAGAAA 427 1333-13-13534 SPP1- 13536 Chl ooooooooooooo 0mm00m00mm000 GCCAGCAACCGAA 428 537-13-13536 SPP1- 13538 Chl ooooooooooooo m0mmmm0m0m0m0 CACCUCACACAUG 429 684-13-13538 SPP1- 13540 Chl ooooooooooooo 00mm000m00m0m AGUUGAAUGGUGC 430 707-13-13540 SPP1- 13542 Chl ooooooooooooo 00mm00mm000m0 AGUCAGCUGGAUG 431 799-13-13542 SPP1- 13544 Chl ooooooooooooo m0m000m000000 UAUAAGCGGAAAG 432 853-13-13544 SPP1- 13546 Chl ooooooooooooo mmmm00m0m00mm UUCCGAUGUGAUU 433 888-13-13546 SPP1- 13548 Chl ooooooooooooo 0m00mm00m0m0m AUAACUAAUGUGU 434 1194-13-13548 SPP1- 13550 Chl ooooooooooooo mm0mmmm0m0000 UCAUUCUAUAGAA 435 1279-13-13550 SPP1- 13552 Chl ooooooooooooo 00mm0mm0mm0m0 AACUAUCACUGUA 436 1300-13-13552 SPP1- 13554 Chl ooooooooooooo 0mm00mm0mmm0m GUCAAUUGCUUAU 437 1510-13-13554 SPP1- 13556 Chl ooooooooooooo 00m00mm00m000 AGCAAUUAAUAAA 438 1543-13-13556 SPP1- 13558 Chl ooooooooooooo 0m00mmmm00m00 ACGACUCUGAUGA 439 4340-13-13558 SPP1- 13560 Chl ooooooooooooo m00m0m00mmm0m UAGUGUGGUUUAU 440 600-13-13560 SPP1- 13562 Chl ooooooooooooo 000mm00m00m00 AAGCCAAUGAUGA 441 863-13-13560 SPP1- 13564 Chl ooooooooooooo 0m00mm00000mm AUAGUCAGGAACU 442 920-13-13564 SPP1- 13566 Chl ooooooooooooo 00mm00mm0m000 AGUCAGCCGUGAA 443 921-13-13566 SPP1- 13568 Chl ooooooooooooo 0mm0mm0m00000 ACUACCAUGAGAA 444 154-13-13568 SPP1- 13570 Chl ooooooooooooo 000m000mm00mm AAACAGGCUGAUU 445 217-13-13570 SPP1- 13572 Chl ooooooooooooo 000m0mm0000mm GAGUGCUGAAACC 446 816-13-13572 SPP1- 13574 Chl ooooooooooooo m000m0mmmm00m UGAGCAUUCCGAU 447 882-13-13572 SPP1- 13576 Chl ooooooooooooo 00mmmm0m00mm0 AAUUCCACAGCCA 448 932-13-13572 SPP1- 13578 Chl ooooooooooooo m0mm00mm0mmm0 UGUCAAUUGCUUA 449 1509-13-13578 SPP1- 13580 Chl ooooooooooooo 0mm0m00000mm0 ACCAUGAGAAUUG 450 157-13-13578 SPP1- 13582 Chl ooooooooooooo mm00m00000mm0 CCAACGAAAGCCA 451 350-13-13582 SPP1- 13584 Chl ooooooooooooo mm00mm0mm00mm CUGGUCACUGAUU 452 511-13-13584 SPP1- 13586 Chl ooooooooooooo m00mmm0m000mm UGGUUUAUGGACU 453 605-13-13586 SPP1- 13588 Chl ooooooooooooo 00mm0000m0mm0 GACCAGAGUGCUG 454 811-13-13588 SPP1- 13590 Chl ooooooooooooo 00m0m00mm00m0 GAUGUGAUUGAUA 455 892-13-13590 SPP1- 13592 Chl ooooooooooooo 0mm00mm0m000m GUCAGCCGUGAAU 456 922-13-13592 SPP1- 13594 Chl ooooooooooooo 00m0m0m0mmm0m AAUGUGUAUCUAU 457 1169-13-13594 SPP1- 13596 Chl ooooooooooooo mm000mmm00000 UUGAGUCUGGAAA 458 1182-13-13596 SPP1- 13598 Chl ooooooooooooo 0mmm00m00mm00 GUCCAGCAAUUAA 459 1539-13-13598 SPP1- 13600 Chl ooooooooooooo mm00m00mm00m0 CCAGCAAUUAAUA 460 1541-13-13600 SPP1- 13602 Chl ooooooooooooo 00mmm000m00mm GACUCGAACGACU 461 427-13-13602 SPP1- 13604 Chl ooooooooooooo 0mmm0mm00m00m ACCUGCCAGCAAC 462 533-13-13604 APOB-- 13763 Chl ooooooooooooo 0m+00+m0+m0+m ACtGAaUAcCAaU 463 13-13763 TEG APOB-- 13764 Chl ooooooooooooo 0mm000m0mm00m ACUGAAUACCAAU 464 13-13764 MAP4K4-- 13766 Chl ooooooooooooo DY547mm0m00000mmm0 CUGUGGAAGUCUA 465 16-13766 PPIB-- 13767 Chl ooooooooooooo mmmmmmmmmmmmm GGCUACAAAAACA 466 13-13767 PPIB-- 13768 Chl ooooooooooooooo mm00mm0m00000m0 UUGGCUACAAAAACA 467 15-13768 PPIB-- 13769 Chl ooooooooooooooo 0mmm00mm0m00000m0 AUUUGGCUACAAAAACA 468 17-13769 oo MAP4K4-- 13939 Chl ooooooooooooo m0m0000m0mmm0 UGUAGGAUGUCUA 469 16-13939 APOB- 13940 Chl ooooooooooooo 0mmm0000000m0 AUCUGGAGAAACA 470 4314-16-13940 APOB- 13941 Chl ooooooooooooooo 000mmm0000000m0 AGAUCUGGAGAAACA 471 4314-17-13941 APOB-- 13942 Chl ooooooooooooo 00mmm0mmm0mm0 GACUCAUCUGCUA 472 16-13942 APOB-- 13943 Chl ooooooooooooo 00mmm0mmm0mm0 GACUCAUCUGCUA 473 16-13943 APOB-- 13944 Chl ooooooooooooooo m000mmm0mmm0mm0 UGGACUCAUCUGCUA 474 17-13944 APOB-- 13945 Chl ooooooooooooooo m000mmm0mmm0mm0 UGGACUCAUCUGCUA 475 19-13945 APOB- 13946 Chl ooooooooooooo 0000000m00m0m GGAGAAACAACAU 476 4314-16-13946 APOB- 13947 Chl ooooooooooooooo mm0000000m00m0m CUGGAGAAACAACAU 477 4314-17-13947 APOB-- 13948 Chl ooooooooooooo 00mmmmmm000m0 AGUCCCUCAAACA 478 16-13948 APOB-- 13949 Chl ooooooooooooooo 0000mmmmmm000m0 AGAGUCCCUCAAACA 479 17-13949 APOB-- 13950 Chl ooooooooooooo 0mm000m0mm00m ACUGAAUACCAAU 480 16-13950 APOB-- 13951 Chl ooooooooooooo 0mm000m0mm00m ACUGAAUACCAAU 481 18-13951 APOB-- 13952 Chl ooooooooooooooo 0m0mm000m0mm00m ACACUGAAUACCAAU 482 17-13952 APOB-- 13953 Chl ooooooooooooooo 0m0mm000m0mm00m ACACUGAAUACCAAU 483 19-13953 MAP4K4-- 13766.2 Chl ooooooooooooo DY547mm0m00000mmm0 CUGUGGAAGUCUA 484 16-13766.2 CTGF- 13980 Chl ooooooooooooo 0m0000000m0m0 ACAGGAAGAUGUA 485 1222-16-13980 CTGF- 13981 Chl ooooooooooooo 000m0000mmmm GAGUGGAGCGCCU 486 813-16-13981 CTGF- 13982 Chl ooooooooooooo m0mm000000m0 CGACUGGAAGACA 487 747-16-13982 CTGF- 13983 Chl ooooooooooooo 0000mmmm0mmm GGAGCGCCUGUUC 488 817-16-13983 CTGF- 13984 Chl ooooooooooooo 0mm0mm0m00mm0 GCCAUUACAACUG 489 1174-16-13984 CTGF- 13985 Chl ooooooooooooo 000mmmmmm00mm GAGCUUUCUGGCU 490 1005-16-13985 CTGF- 13986 Chl ooooooooooooo 00m0000mmmm0 AGUGGAGCGCCUG 491 814-16-13986 CTGF- 13987 Chl ooooooooooooo m0000mmmm0mm UGGAGCGCCUGUU 492 816-16-13987 CTGF- 13988 Chl ooooooooooooo 0mmm000mmmmmm GUUUGAGCUUUCU 493 1001-16-13988 CTGF- 13989 Chl ooooooooooooo m0mm0mm0m00mm UGCCAUUACAACU 494 1173-16-13989 CTGF- 13990 Chl ooooooooooooo 0mm000000m0m ACUGGAAGACACG 495 749-16-13990 CTGF- 13991 Chl ooooooooooooo 00mm0mmm00mmm AACUGCCUGGUCC 496 792-16-13991 CTGF- 13992 Chl ooooooooooooo 000mmm0m0mmm0 AGACCUGUGCCUG 497 1162-16-13992 CTGF- 13993 Chl ooooooooooooo m0000m0000mm CAGAGUGGAGCGC 498 811-16-13993 CTGF- 13994 Chl ooooooooooooo mmm00mmm000mm CCUGGUCCAGACC 499 797-16-13994 CTGF- 13995 Chl ooooooooooooo mm0mm0m00mm0m CCAUUACAACUGU 500 1175-16-13995 CTGF- 13996 Chl ooooooooooooo mm0mm0mm0m00m CUGCCAUUACAAC 501 1172-16-13996 CTGF- 13997 Chl ooooooooooooo 0mm0m00mm0mmm AUUACAACUGUCC 502 1177-16-13997 CTGF- 13998 Chl ooooooooooooo m0mm0m00mm0mm CAUUACAACUGUC 503 1176-16-13998 CTGF- 13999 Chl ooooooooooooo 0000m0000mmm AGAGUGGAGCGCC 504 812-16-13999 CTGF- 14000 Chl ooooooooooooo 0mm0mm000000 ACCGACUGGAAGA 505 745-16-14000 CTGF- 14001 Chl ooooooooooooo 0m0m0m0000m0 AUGUACGGAGACA 506 1230-16-14001 CTGF- 14002 Chl ooooooooooooo 0mmmm0m000mm GCCUUGCGAAGCU 507 920-16-14002 CTGF- 14003 Chl ooooooooooooo 0mm0m00000m0 GCUGCGAGGAGUG 508 679-16-14003 CTGF- 14004 Chl ooooooooooooo 0mmm0mm000mmm GCCUAUCAAGUUU 509 992-16-14004 CTGF- 14005 Chl ooooooooooooo 00mmmm0m0000m AAUUCUGUGGAGU 510 1045-16-14005 CTGF- 14006 Chl ooooooooooooo m0m0m0000m0m UGUACGGAGACAU 511 1231-16-14006 CTGF- 14007 Chl ooooooooooooo 00mmm0mm000mm AGCCUAUCAAGUU 512 991-16-14007 CTGF- 14008 Chl ooooooooooooo m000mmm000mmm CAAGUUUGAGCUU 513 998-16-14008 CTGF- 14009 Chl ooooooooooooo mm0m0000m0m0m CUGUGGAGUAUGU 514 1049-16-14009 CTGF- 14010 Chl ooooooooooooo 000mmmm0m0000 AAAUUCUGUGGAG 515 1044-16-14010 CTGF- 14011 Chl ooooooooooooo mmmm00m00m0m0 UUUCAGUAGCACA 516 1327-16-14011 CTGF- 14012 Chl ooooooooooooo m00m00m0mmmmm CAAUGACAUCUUU 517 1196-16-14012 CTGF- 14013 Chl ooooooooooooo 00m0mm00m0m0m AGUACCAGUGCAC 518 562-16-14013 CTGF- 14014 Chl ooooooooooooo 000000m0mmmm GGAAGACACGUUU 519 752-16-14014 CTGF- 14015 Chl ooooooooooooo mm0mm000mmm00 CUAUCAAGUUUGA 520 994-16-14015 CTGF- 14016 Chl ooooooooooooo 00mm000mmmm0m AGCUAAAUUCUGU 521 1040-16-14016 CTGF- 14017 Chl ooooooooooooo 000m0000m0m00 AGGUAGAAUGUAA 522 1984-16-14017 CTGF- 14018 Chl ooooooooooooo 00mm00mm00mmm AGCUGAUCAGUUU 523 2195-16-14019 CTGF- 14019 Chl ooooooooooooo mmmm0mmm000m0 UUCUGCUCAGAUA 524 2043-16-14019 CTGF- 14020 Chl ooooooooooooo mm0mmm000mm00 UUAUCUAAGUUAA 525 1892-16-14020 CTGF- 14021 Chl ooooooooooooo m0m0m00m00m0 UAUACGAGUAAUA 526 156-16-14021 CTGF- 14022 Chl ooooooooooooo 00mm000m00mmm GACUGGACAGCUU 527 1780-16-14022 CTGF- 14023 Chl ooooooooooooo 0m00mmmmm0mm0 AUGGCCUUUAUUA 528 2162-16-14023 CTGF- 14024 Chl ooooooooooooo 0m0mm00mm000 AUACCGAGCUAAA 529 1034-16-14024 CTGF- 14025 Chl ooooooooooooo mm0mm00000m0m UUGUUGAGAGUGU 530 2264-16-14025 CTGF- 14026 Chl ooooooooooooo 0m0m0mm00mm0 ACAUACCGAGCUA 531 1032-16-14026 CTGF- 14027 Chl ooooooooooooo 00m0000000mm0 AGCAGAAAGGUUA 532 1535-16-14027 CTGF- 14028 Chl ooooooooooooo 00mm0mmmmmm00 AGUUGUUCCUUAA 533 1694-13-14028 CTGF- 14029 Chl ooooooooooooo 0mmm0000m0m00 AUUUGAAGUGUAA 534 1588-16-14029 CTGF- 14030 Chl ooooooooooooo 000mm00mmm000 AAGCUGACCUGGA 535 928-16-14030 CTGF- 14031 Chl ooooooooooooo 00mm0m0000000 GGUCAUGAAGAAG 536 1133-16-14031 CTGF- 14032 Chl ooooooooooooo 0m00mm000mmmm AUGGUCAGGCCUU 537 912-16-14032 CTGF- 14033 Chl ooooooooooooo 00000m0mmmm0 GAAGACACGUUUG 538 753-16-14033 CTGF- 14034 Chl ooooooooooooo 000mmmm0m000 AGGCCUUGCGAAG 539 918-16-14034 CTGF- 14035 Chl ooooooooooooo m0mm0mm00000 UACCGACUGGAAG 540 744-16-14035 CTGF- 14036 Chl ooooooooooooo 0mmm0000mm0 ACCGCAAGAUCGG 541 466-16-14036 CTGF- 14037 Chl ooooooooooooo m000mmmm0m00 CAGGCCUUGCGAA 542 917-16-10437 CTGF- 14038 Chl ooooooooooooo m00mm000mmmm CGAGCUAAAUUCU 543 1038-16-14038 CTGF- 14039 Chl ooooooooooooo mmm0m0000m0m0 UCUGUGGAGUAUG 544 1048-16-14039 CTGF- 14040 Chl ooooooooooooo m0000m0m00m0 CGGAGACAUGGCA 545 1235-16-14040 CTGF- 14041 Chl ooooooooooooo 0m00m00mmmmm AUGACAACGCCUC 546 868-16-14041 CTGF- 14042 Chl ooooooooooooo 0000mm0m00000 GAGGUCAUGAAGA 547 1131-16-14042 CTGF- 14043 Chl ooooooooooooo m000mmmm0m000 UAAAUUCUGUGGA 548 1043-16-14043 CTGF- 14044 Chl ooooooooooooo m000000m0mmm UGGAAGACACGUU 549 751-16-14044 CTGF- 14045 Chl ooooooooooooo 0000m0m0m000 AAGAUGUACGGAG 550 1227-16-14045 CTGF- 14046 Chl ooooooooooooo 00m00m00mmmm AAUGACAACGCCU 551 867-16-14046 CTGF- 14047 Chl ooooooooooooo 00m000mm0m00 GGCGAGGUCAGA 552 1128-16-14047 CTGF- 14048 Chl ooooooooooooo 00m0m0mmm00mm GACACGUUUGGCC 553 756-16-14048 CTGF- 14049 Chl ooooooooooooo 0m00000m0m00m ACGGAGACAUGGC 554 1234-16-14049 CTGF- 14050 Chl ooooooooooooo mm000mmmm0m00 UCAGGCCUUGCGA 555 916-16-14050 CTGF- 14051 Chl ooooooooooooo 0m0000mm00mmm GCGAAGCUGACCU 556 925-16-14051 CTGF- 14052 Chl ooooooooooooo 000000m0m0m00 GGAAGAUGUACGG 557 1225-16-14052 CTGF- 14053 Chl ooooooooooooo 0m00mmmm00mmm GUGACUUCGGCUC 558 445-16-14053 CTGF- 14054 Chl ooooooooooooo m00mmmm00mmmm UGACUUCGGCUCC 559 446-16-10454 CTGF- 14055 Chl ooooooooooooo m00mm000mmmm0 UGGUCAGGCCUUG 560 913-16-14055 CTGF- 14056 Chl ooooooooooooo mm000mmm000mm UCAAGUUUGAGCU 561 997-16-14056 CTGF- 14057 Chl ooooooooooooo 0mm0000mm0m00 GCCAGAACUGCAG 562 277-16-14057 CTGF- 14058 Chl ooooooooooooo m0000m0m0m0mm UGGAGUAUGUACC 563 1052-16-14058 CTGF- 14059 Chl ooooooooooooo 0mm0000000m00 GCUAGAGAAGCAG 564 887-16-14059 CTGF- 14060 Chl ooooooooooooo 00mm000mmmm0m GGUCAGGCCUUGC 565 914-16-14060 CTGF- 14061 Chl ooooooooooooo 000mm000mmmm0 GAGCUAAAUUCUG 566 1039-16-14061 CTGF- 14062 Chl ooooooooooooo 0000m0m0mmm00 AAGACACGUUUGG 567 754-16-14062 CTGF- 14063 Chl ooooooooooooo m0000mm0m0000 CGAGGUCAUGAAG 568 1130-16-14063 CTGF- 14064 Chl ooooooooooooo 00mmmm0m0000m GGCCUUGCGAAGC 569 919-16-14064 CTGF- 14065 Chl ooooooooooooo mmm0m0000mm00 CUUGCGAAGCUGA 570 922-16-14065 CTGF- 14066 Chl ooooooooooooo mm00mm000000m CCGACUGGAAGAC 571 746-16-14066 CTGF- 14067 Chl ooooooooooooo mmm0mm000mmm0 CCUAUCAAGUUUG 572 993-16-14067 CTGF- 14068 Chl ooooooooooooo m0mmmm0000mmm UGUUCCAAGACCU 573 825-16-14068 CTGF- 14069 Chl ooooooooooooo m0000mm00mmm0 CGAAGCUGACCUG 574 926-16-14069 CTGF- 14070 Chl ooooooooooooo mm0m0000mm00m UUGCGAAGCUGAC 575 923-16-14070 CTGF- 14071 Chl ooooooooooooo m00m00m00m0mm CAAUGACAACGCC 576 866-16-14071 CTGF- 14072 Chl ooooooooooooo 0m0mm00m0m0m0 GUACCAGUGCACG 577 563-16-14072 CTGF- 14073 Chl ooooooooooooo mmm0mmmm0000m CCUGUUCCAAGAC 578 823-16-14073 CTGF- 14074 Chl ooooooooooooo m0m00000m0m00 UACGGAGACAUGG 579 1233-16-14074 CTGF- 14075 Chl ooooooooooooo m0m0000mm00mm UGCGAAGCUGACC 580 924-16-14075 CTGF- 14076 Chl ooooooooooooo mmmm0m0000mm0 CCUUGCGAAGCUG 581 921-16-10476 CTGF- 14077 Chl ooooooooooooo mm0m00mmmm00m CUGUGACUUCGGC 582 443-16-14077 CTGF- 14078 Chl ooooooooooooo 0mm000mmmm0m0 GCUAAAUUCUGUG 583 1041-16-14078 CTGF- 14079 Chl ooooooooooooo mm000mmmm0m00 CUAAAUUCUGUGG 584 1042-16-14079 CTGF- 14080 Chl ooooooooooooo 000m0m0mmm00m AGACACGUUUGGC 585 755-16-14079 CTGF- 14081 Chl ooooooooooooo mm0m0000mm00m CCGCAAGAUCGGC 586 467-16-14081 CTGF- 14082 Chl ooooooooooooo m0mm000mmm000 UAUCAAGUUUGAG 587 995-16-14082 CTGF- 14083 Chl ooooooooooooo 0000mm00mmm00 GAAGCUGACCUGG 588 927-16-14083 SPP1- 14131 Chl ooooooooooooo 0m0mmm00mm000 GCAUUUAGUCAAA 589 1091-16-14131 PPIB-- 14188 Chl ooooooooooooo mmmmmmmmmmmmm GGCUACAAAAACA 590 16-14188 PPIB-- 14189 Chl ooooooooooooooo mm00mm0m00000m0 UUGGCUACAAAAACA 591 17-14189 PPIB-- 14190 Chl ooooooooooooooo 0mmm00mm0m00000m0 AUUUGGCUACAAAAACA 592 18-14190 oo pGL3- 14386 chl ooooooooooooo 0m000m0m00mmm ACAAAUACGAUUU 593 1172-16-14386 pGL3- 14387 chl ooooooooooooo DY5470m000m0m00mmm ACAAAUACGAUUU 594 1172-16-14387 MAP4K4- 14390 Chl ooooooooooooooo Pmmmmmmmmmmmm000mm CUUUGAAGAGUUCUGUGGAAG 595 2931-25-14390 oooooooooo mmmmmmmm UCUA miR- 14391 Chl ssooooooooooooo mmmmmmmmmmmmmmmmmm ACAAACACCAUUGUCACACUC 596 122--23-14391 oooossss mmmmm CA 14084 Chl ooooooooooooo mmm0m000mm000 CUCAUGAAUUAGA 719 14085 Chl ooooooooooooo mm0000mm00mm0 CUGAGGUCAAUUA 720 14086 Chl ooooooooooooo 0000mm00mm000 GAGGUCAAUUAAA 721 14087 Chl ooooooooooooo mmm0000mm00mm UCUGAGGUCAAUU 722 14088 Chl ooooooooooooo m0000mm00mm00 UGAGGUCAAUUAA 723 14089 Chl ooooooooooooo mmmm0000mm00m UUCUGAGGUCAAU 724 14090 Chl ooooooooooooo 0mm00mm000m00 GUCAGCUGGAUGA 725 14091 Chl ooooooooooooo mmmm0m000mmm UUCUGAUGAAUCU 726 14092 Chl ooooooooooooo m000mm0000mm0 UGGACUGAGGUCA 727 14093 Chl ooooooooooooo 000mmmm0mm0mm GAGUCUCACCAUU 728 14094 Chl ooooooooooooo 00mm0000mm000 GACUGAGGUCAAA 729 14095 Chl ooooooooooooo mm0m00mm0m000 UCACAGCCAUGAA 730 14096 Chl ooooooooooooo 00mmmm0mm0mmm AGUCUCACCAUUC 731 14097 Chl ooooooooooooo 000m00000mm0 AAGCGGAAAGCCA 732 14098 Chl ooooooooooooo 00m00000mm00 AGCGGAAAGCCAA 733 14099 Chl ooooooooooooo 0mm0m0m000m00 ACCACAUGGAUGA 734 14100 Chl ooooooooooooo 0mm0m00mm0m0m GCCAUGACCACAU 735 14101 Chl ooooooooooooo 000mm0m00mm0m AAGCCAUGACCAC 736 14102 Chl ooooooooooooo 0m00000mm00m GCGGAAAGCCAAU 737 14103 Chl ooooooooooooo 000mmmmm0mmm AAAUUUCGUAUUU 738 14104 Chl ooooooooooooo 0mmmmm0mmmmm AUUUCGUAUUUCU 739 14105 Chl ooooooooooooo 0000mm0m00mm0 AAAGCCAUGACCA 740 14106 Chl ooooooooooooo 0m0m000m00m0m ACAUGGAUGAUAU 741 14107 Chl ooooooooooooo 0000mmmmm0mm GAAAUUUCGUAUU 742 14108 Chl ooooooooooooo 0mmmmmmm00mm GCGCCUUCUGAUU 743 14109 Chl ooooooooooooo 0mmmmmm0m000m AUUUCUCAUGAAU 744 14110 Chl ooooooooooooo mmmmm0m000m00 CUCUCAUGAAUAG 745 14111 Chl ooooooooooooo 000mmm00m000 AAGUCCAACGAAA 746 14112 Chl ooooooooooooo 0m00m00000m00 AUGAUGAGAGCAA 747 14113 Chl ooooooooooooo 0m00000mm000 GCGAGGAGUUGAA 748 14114 Chl ooooooooooooo m00mm00m00mm0 UGAUUGAUAGUCA 749 14115 Chl ooooooooooooo 000m00m0m0mmm AGAUAGUGCAUCU 750 14116 Chl ooooooooooooo 0m0m0m0mmm0mm AUGUGUAUCUAUU 751 14117 Chl ooooooooooooo mmmm0m0000000 UUCUAUAGAAGAA 752 14118 Chl ooooooooooooo mm0mmm00m00mm UUGUCCAGCAAUU 753 14119 Chl ooooooooooooo 0m0m000000m0 ACAUGGAAAGCGA 754 14120 Chl ooooooooooooo 0m00mmm000mm0 GCAGUCCAGAUUA 755 14121 Chl ooooooooooooo m00mm000m0m0m UGGUUGAAUGUGU 756 14122 Chl ooooooooooooo mm0m0000m00m UUAUGAAACGAGU 757 14123 Chl ooooooooooooo m00mmm000mm0m CAGUCCAGAUUAU 758 14124 Chl ooooooooooooo 0m0m000m0000 AUAUAAGCGGAAA 759 14125 Chl ooooooooooooo m0mm00mm000m0 UACCAGUUAAACA 760 14126 Chl ooooooooooooo m0mmm0mmmm0m0 UGUUCAUUCUAUA 761 14127 Chl ooooooooooooo mm0mm0000000 CCGACCAAGGAAA 762 14128 Chl ooooooooooooo 000m00m0m0m0m GAAUGGUGCAUAC 763 14129 Chl ooooooooooooo 0m0m00m00mm0 AUAUGAUGGCCGA 764 14130 Chl ooooooooooooo 00m00mmm000mm AGCAGUCCAGAUU 765 14132 Chl ooooooooooooo 00m0mmmm0m0m AGCAUUCCGAUGU 766 14133 Chl ooooooooooooo m00mm00000mmm UAGUCAGGAACUU 767 14134 Chl ooooooooooooo m0m0mmm00mm00 UGCAUUUAGUCAA 768 14135 Chl ooooooooooooo 0mmm00m000mmm GUCUGAUGAGUCU 769 14136 Chl ooooooooooooo m000m0m0m0m00 UAGACACAUAUGA 770 14137 Chl ooooooooooooo m000m0000m0m CAGACGAGGACAU 771 14138 Chl ooooooooooooo m00mmm000mmm CAGCCGUGAAUUC 772 14139 Chl ooooooooooooo 00mmm00000m00 AGUCUGGAAAUAA 773 14140 Chl ooooooooooooo 00mmm0m00mmmm AGUUUGUGGCUUC 774 14141 Chl ooooooooooooo 00mmm00m0000 AGUCCAACGAAAG 775 14142 Chl ooooooooooooo 000mmmmm000m AAGUUUCGCAGAC 776 14143 Chl ooooooooooooo 00m00m000m0mm AGCAAUGAGCAUU 777 14144 Chl ooooooooooooo mm000m00m0m0m UUAGAUAGUGCAU 778 14145 Chl ooooooooooooo m00m0m0m0m000 UGGUGCAUACAAG 779 14146 Chl ooooooooooooo 0m0000m00mm0 AUGAAACGAGUCA 780 14147 Chl ooooooooooooo mm0000m0mm000 CCAGAGUGCUGAA 781 14148 Chl ooooooooooooo m00mm0m000mmm CAGCCAUGAAUUU 782 14149 Chl ooooooooooooo 0mm00mm000m0m AUUGGUUGAAUGU 783 14150 Chl ooooooooooooo 00mm000m0m0m0 GGUUGAAUGUGUA 784 14151 Chl ooooooooooooo 00000m00mm00m GGAAAUAACUAAU 785 14152 Chl ooooooooooooo mm0m000m00000 UCAUGAAUAGAAA 786 14153 Chl ooooooooooooo 0mm00m00mm00 GCCAGCAACCGAA 787 14154 Chl ooooooooooooo m0mmmm0m0m0m0 CACCUCACACAUG 788 14155 Chl ooooooooooooo 00mm000m00m0m AGUUGAAUGGUGC 789 14156 Chl ooooooooooooo 00mm00mm000m0 AGUCAGCUGGAUG 790 14157 Chl ooooooooooooo m0m000m00000 UAUAAGCGGAAAG 791 14158 Chl ooooooooooooo mmmm0m0m00mm UUCCGAUGUGAUU 792 14159 Chl ooooooooooooo 0m00mm00m0m0m AUAACUAAUGUGU 793 14160 Chl ooooooooooooo mm0mmmm0m0000 UCAUUCUAUAGAA 794 14161 Chl ooooooooooooo 00mm0mm0mm0m0 AACUAUCACUGUA 795 14162 Chl ooooooooooooo 0mm00mm0mmm0m GUCAAUUGCUUAU 796 14163 Chl ooooooooooooo 00m00mm00m000 AGCAAUUAAUAAA 797 14164 Chl ooooooooooooo 0m0mmmm00m00 ACGACUCUGAUGA 798 14165 Chl ooooooooooooo m00m0m00mmm0m UAGUGUGGUUUAU 799 14166 Chl ooooooooooooo 000mm00m00m00 AAGCCAAUGAUGA 800 14167 Chl ooooooooooooo 0m00mm00000mm AUAGUCAGGAACU 801 14168 Chl ooooooooooooo 00mm00mmm000 AGUCAGCCGUGAA 802 14169 Chl ooooooooooooo 0mm0mm0m00000 ACUACCAUGAGAA 803 14170 Chl ooooooooooooo 000m000mm00mm AAACAGGCUGAUU 804 14171 Chl ooooooooooooo 000m0mm0000mm GAGUGCUGAAACC 805 14172 Chl ooooooooooooo m000m0mmmm0m UGAGCAUUCCGAU 806 17173 Chl ooooooooooooo 00mmmm0m00mm0 AAUUCCACAGCCA 807 14174 Chl ooooooooooooo m0mm00mm0mmm0 UGUCAAUUGCUUA 808 14175 Chl ooooooooooooo 0mm0m00000mm0 ACCAUGAGAAUUG 809 14176 Chl ooooooooooooo mm00m0000mm0 CCAACGAAAGCCA 810 14177 Chl ooooooooooooo mm00mm0mm00mm CUGGUCACUGAUU 811 14178 Chl ooooooooooooo m00mmm0m000mm UGGUUUAUGGACU 812 14179 Chl ooooooooooooo 00mm0000m0mm0 GACCAGAGUGCUG 813 14180 Chl ooooooooooooo 00m0m00mm00m0 GAUGUGAUUGAUA 814 14181 Chl ooooooooooooo 0mm00mmm000m GUCAGCCGUGAAU 815 14182 Chl ooooooooooooo 00m0m0m0mmm0m AAUGUGUAUCUAU 816 14183 Chl ooooooooooooo mm000mmm00000 UUGAGUCUGGAAA 817 14184 Chl ooooooooooooo 0mmm00m00mm00 GUCCAGCAAUUAA 818 14185 Chl ooooooooooooo mm00m00mm00m0 CCAGCAAUUAAUA 819 14186 Chl ooooooooooooo 00mmm00m0mm GACUCGAACGACU 820 14187 Chl ooooooooooooo 0mmm0mm00m00m ACCUGCCAGCAAC 821 Sense backbone, chemistry, and sequence information. o: phosphodiester; s: phosphorothioate; P: 5' phosphorylation; 0: 2'-OH; F: 2'-fluror; m: 2' O-methyl; +: LNA modification. Capital letters in the sequence signify ribonucleotides, lower case letters signify deoxyribonucleotides. Having thus described several aspects of at least one embodiment of this invention, it is to be appreciated various alterations, modifications, and improvements will readily occur to those skilled in the art. Such alterations, modifications, and improvements are intended to be part of this disclosure, and are intended to be within the spirit and scope of the invention. Accordingly, the foregoing description and drawings are by way of example only.

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.

All references, including patent documents, disclosed herein are incorporated by reference in their entirety. This application incorporates by reference the entire contents, including all the drawings and all parts of the specification (including sequence listing or amino acid/polynucleotide sequences) of the co-pending U.S. Provisional Application No. 61/135,855, filed on Jul. 24, 2008, entitled “SHORT HAIRPIN RNAI CONSTRUCTS AND USES THEROF,” and U.S. Provisional Application No. 61/197,768, filed on Oct. 30, 2008, entitled “MINIRNA CONSTRUCTS AND USES THEREOF.” 

What is claimed is: 1-6. (canceled)
 7. A method for treating or preventing a fibrotic disorder in a subject in need thereof, the method comprising: administering to the subject a therapeutically effective amount for treating or preventing a fibrotic disorder of a double stranded nucleic acid molecule comprising a guide strand, with a minimal length of 16 nucleotides, and a passenger strand forming a double stranded nucleic acid, having a double stranded region and a single stranded region, the double stranded region having 8-15 nucleotides in length, the single stranded region having 4-12 nucleotides in length, wherein the single stranded region comprises 2-12 phosphorothioate modifications, wherein at least 40% of the nucleotides of the double stranded nucleic acid molecule are modified, and wherein the double stranded nucleic acid molecule is directed against COX-2. 8-15. (canceled)
 16. The method of claim 7, wherein the double stranded nucleic acid molecule is administered via intradermal injection.
 17. The method of claim 16, wherein the double stranded nucleic acid molecule is administered via local administration to the skin. 18-25. (canceled)
 26. The method of claim 7, wherein the double stranded nucleic acid molecule is administered on the skin of the subject in need thereof.
 27. The method of claim 26, wherein the double stranded nucleic acid molecule is in the form of a cream or ointment.
 28. The method of claim 7, wherein the double stranded nucleic acid molecule is administered by local injection. 29-31. (canceled)
 32. The method of claim 7, wherein the fibrotic disorder is selected from the group consisting of pulmonary fibrosis, liver cirrhosis, scleroderma, glomerulonephritis, lung fibrosis, liver fibrosis, skin fibrosis, muscle fibrosis, radiation fibrosis, kidney fibrosis, proliferative vitreoretinopathy, and uterine fibrosis.
 33. The method of claim 7, wherein the single stranded region contains 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 phosphorothioate modifications.
 34. The method of claim 7, wherein the double stranded nucleic acid molecule comprises a hydrophobic conjugate attached to the guide strand or the passenger strand.
 35. The method of claim 34, wherein the conjugate is cholesterol.
 36. The method of claim 7, wherein at least one of the nucleotides of the isolated double stranded nucleic acid molecule that is modified comprises a 2′O-methyl or a 2′O-fluoro modification.
 37. The method of claim 7, wherein at least one of the nucleotides of the isolated double stranded nucleic acid molecule that is modified comprises a hydrophobic modification.
 38. The method of claim 7, wherein the double stranded region is 11, 12, 13, or 14 nucleotides long.
 39. The method of claim 7, wherein each nucleotide within the single stranded region has a phosphorothioate modification.
 40. The method of claim 34, wherein the hydrophobic conjugate is attached to the double stranded nucleic acid molecule through a linker.
 41. The method of claim 41, wherein the linker is a TEG linker.
 42. The method of claim 7, wherein the single stranded region is at least 4, at least 5, or at least 6 nucleotides long. 